A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982779



Internal ID18617974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125915974..125919565hg38UCSC Ensembl
Innerchr10:127604543..127608134hg19UCSC Ensembl
Innerchr10:127594533..127598124hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383592
hg193592
hg183592
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2616315, nssv2616313, nssv2616308, nssv2616316, nssv2616311, nssv2616312, nssv2616309, nssv2616310, nssv2616317, nssv2616314
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFANK1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982779
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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