A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966775



Internal ID18602005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34935250..34972877hg38UCSC Ensembl
Innerchr7:34974862..35012489hg19UCSC Ensembl
Innerchr7:34941387..34979014hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3837628
hg1937628
hg1837628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2441382, nssv2441380, nssv2441383, nssv2441381, nssv2441377, nssv2441378, nssv2441384, nssv2441385, nssv2441376, nssv2441379
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDPY19L1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966775
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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