A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981471



Internal ID18616668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55470712..55473099hg38UCSC Ensembl
Innerchr7:55538405..55540792hg19UCSC Ensembl
Innerchr7:55505899..55508286hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg382388
hg192388
hg182388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2448466, nssv2448465, nssv2448464, nssv2448462, nssv2448469, nssv2448470, nssv2448467, nssv2448471, nssv2448468, nssv2448463
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesVOPP1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981471
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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