A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947741



Internal ID18594588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13157506..13160019hg38UCSC Ensembl
Innerchr10:13199506..13202019hg19UCSC Ensembl
Innerchr10:13239512..13242025hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382514
hg192514
hg182514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832404, nssv1832400, nssv1832396, nssv1832405, nssv1832401, nssv1832399, nssv1832398, nssv1832402, nssv1832397, nssv1832403
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947741
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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