A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517063



Internal ID15444356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29162255..31275690hg38UCSC Ensembl
Innerchr9:29162253..31275688hg19UCSC Ensembl
Innerchr9:29152253..31265688hg18UCSC Ensembl
Innerchr9:29152253..31265688hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382113436
hg192113436
hg182113436
hg172113436
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv693203, nssv685678, nssv654557, nssv663099, nssv699166, nssv652644, nssv659679, nssv700363, nssv689694, nssv690362, nssv655492, nssv683908, nssv658084, nssv663270, nssv655393, nssv687761, nssv685611, nssv703846, nssv703368, nssv653199, nssv677997, nssv670672, nssv671733, nssv695271, nssv666272, nssv653564, nssv654175, nssv660606, nssv687018, nssv693653, nssv669083, nssv660465, nssv670524, nssv667103, nssv674502, nssv653380, nssv686214, nssv693345, nssv672881, nssv687312, nssv689162, nssv684204, nssv689991, nssv701983, nssv697392, nssv704262, nssv679312, nssv657333, nssv671424, nssv689793, nssv696817, nssv653877, nssv670977, nssv672607
Samples
Known GenesLINGO2, LOC401497
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517063
Frequency
Sample Size2026
Observed Gain10
Observed Loss44
Observed Complex0
Frequencyn/a


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