A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947816



Internal ID18594663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31360507..31364251hg38UCSC Ensembl
Innerchr10:31649436..31653180hg19UCSC Ensembl
Innerchr10:31689442..31693186hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg383745
hg193745
hg183745
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1836736, nssv1836732, nssv1836734, nssv1836731, nssv1836733, nssv1836729, nssv1836735, nssv1836737, nssv1836728, nssv1836730
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZEB1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947816
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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