A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965700



Internal ID18600930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27877736..27880987hg38UCSC Ensembl
Innerchr6:27845514..27848765hg19UCSC Ensembl
Innerchr6:27953493..27956744hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383252
hg193252
hg183252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2399367, nssv2399372, nssv2399373, nssv2399368, nssv2399365, nssv2399366, nssv2399374, nssv2399369, nssv2399370, nssv2399371
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)nsv965700
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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