A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981567



Internal ID18616764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103210545..103284387hg38UCSC Ensembl
Innerchr7:102850992..102924834hg19UCSC Ensembl
Innerchr7:102638228..102712070hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3873843
hg1973843
hg1873843
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2473743, nssv2473748, nssv2473745, nssv2473744, nssv2473747, nssv2473742, nssv2473741, nssv2473746, nssv2473740, nssv2473749
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDPY19L2P2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981567
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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