A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947910



Internal ID18594756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45620923..45624256hg38UCSC Ensembl
Innerchr10:46116371..46119704hg19UCSC Ensembl
Innerchr10:45436377..45439710hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383334
hg193334
hg183334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1844246, nssv1844251, nssv1844249, nssv1844254, nssv1844247, nssv1844245, nssv1844250, nssv1844248, nssv1844252, nssv1844253
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZFAND4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947910
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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