A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091649



Internal ID15598149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99927618..100004568hg38UCSC Ensembl
Innerchr7:99525241..99602191hg19UCSC Ensembl
Innerchr7:99363177..99440127hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3876951
hg1976951
hg1876951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607930
Supporting Variants
Samples
Known GenesAZGP1, AZGP1P1, GJC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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