A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947823



Internal ID18594670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:32944835..32946503hg38UCSC Ensembl
Innerchr10:33233763..33235431hg19UCSC Ensembl
Innerchr10:33273769..33275437hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381669
hg191669
hg181669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1839161, nssv1839158, nssv1839156, nssv1839160, nssv1839154, nssv1839159, nssv1839155, nssv1839157, nssv1839162, nssv1839163
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesITGB1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947823
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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