A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947739



Internal ID18247900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13057457..13059128hg38UCSC Ensembl
Innerchr10:13099457..13101128hg19UCSC Ensembl
Innerchr10:13139463..13141134hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381672
hg191672
hg181672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1831285, nssv1831286, nssv1831287, nssv1831282, nssv1831280, nssv1831278, nssv1831283, nssv1831279, nssv1831281, nssv1831284
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCCDC3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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