A curated catalogue of human genomic structural variation

Variant Details

Variant: nsv516763

Internal ID

15444056

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr10:20494784..20573498	hg38	UCSC Ensembl
Inner	chr10:20783713..20862427	hg19	UCSC Ensembl
Inner	chr10:20823719..20902433	hg18	UCSC Ensembl
Inner	chr10:20823719..20902433	hg17	UCSC Ensembl

Cytoband

10p12.31

Allele length

Assembly	Allele length
hg38	78715
hg19	78715
hg18	78715
hg17	78715

Variant Type

CNV gain+loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

M

Merged Variants

Supporting Variants

nssv681438, nssv664971, nssv693181, nssv689112, nssv691710, nssv674043, nssv692186, nssv655227, nssv664865, nssv663410, nssv678660, nssv669333, nssv667960, nssv689564, nssv665682, nssv652704, nssv691934, nssv689414, nssv652318, nssv655623, nssv670528, nssv668239, nssv670059, nssv662677, nssv658589, nssv687542, nssv686414, nssv656111, nssv653716, nssv661314, nssv653276, nssv688366, nssv693025, nssv691578, nssv655658, nssv688809, nssv680640, nssv690279, nssv681243, nssv653939, nssv692048, nssv683530, nssv668697, nssv670927, nssv667043, nssv675124, nssv676567, nssv686175, nssv656319, nssv676138, nssv663918, nssv690436, nssv677168, nssv666013, nssv662899, nssv658165, nssv691894, nssv665758, nssv686395, nssv652972, nssv689371, nssv686439, nssv652921, nssv683556, nssv681761, nssv685770, nssv687763, nssv702284, nssv677687, nssv653110, nssv688600, nssv687904, nssv671255, nssv665857, nssv691617, nssv685741, nssv677294, nssv700404, nssv676230, nssv702996, nssv686128, nssv680610, nssv664575, nssv652006, nssv663347, nssv663037, nssv687687, nssv680581, nssv688713, nssv673841, nssv688101, nssv652360, nssv687952, nssv682998, nssv676515, nssv660167, nssv683503, nssv664180, nssv655546, nssv692772, nssv692355, nssv686016, nssv683459, nssv672388, nssv678961, nssv677466, nssv663368, nssv658408, nssv691098, nssv655705, nssv671102, nssv684539, nssv673891, nssv663606, nssv684144, nssv676539, nssv682315, nssv656911, nssv685790, nssv688437, nssv653453, nssv689621, nssv668527, nssv658992, nssv663437, nssv690507, nssv689698, nssv669826, nssv685633, nssv687747, nssv677487, nssv670280, nssv693992, nssv668398, nssv658425, nssv677079, nssv670684, nssv661345, nssv692829, nssv682550, nssv655836, nssv688830, nssv668092, nssv687660, nssv688183, nssv662854, nssv664274, nssv653669, nssv672234, nssv653529, nssv679534, nssv668874, nssv689883, nssv687342, nssv692416, nssv686155, nssv681401, nssv666712, nssv657452, nssv675997, nssv668328, nssv659365, nssv677783, nssv689535, nssv687713, nssv670578, nssv670978, nssv677210, nssv671426, nssv668917, nssv693367, nssv693346, nssv681015, nssv676351, nssv656581, nssv675957, nssv671285, nssv684329, nssv673136, nssv687315, nssv688736, nssv655517, nssv685529, nssv674522, nssv692593, nssv660098, nssv683819, nssv676890, nssv673499

Samples

Known Genes

Method

SNP array

Analysis

Sample-level CNVs

Platform

GPL6434

Comments

Reference

Shaikh_et_al_2009

Pubmed ID

Accession Number(s)

Frequency

Sample Size	2026
Observed Gain	31
Observed Loss	159
Observed Complex	0
Frequency	n/a