A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966829



Internal ID18602059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65936971..65943487hg38UCSC Ensembl
Innerchr7:65401958..65408474hg19UCSC Ensembl
Innerchr7:65039393..65045909hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg386517
hg196517
hg186517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2458545, nssv2458544, nssv2458543, nssv2458540, nssv2458539, nssv2458538, nssv2458537, nssv2458541, nssv2458536, nssv2458542
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesVKORC1L1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966829
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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