A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674762



Internal ID18626357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158599839..158669417hg38UCSC Ensembl
Innerchr7:158392531..158462109hg19UCSC Ensembl
Innerchr7:158085292..158154870hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3869579
hg1969579
hg1869579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032713
Supporting Variants
Samples
Known GenesNCAPG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674762
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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