A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029800



Internal ID19119019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65844340..65902705hg38UCSC Ensembl
Innerchr7:65309327..65367692hg19UCSC Ensembl
Innerchr7:64946762..65005127hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3858366
hg1958366
hg1858366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655625
Samples
Known GenesVKORC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029800
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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