A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699798



Internal ID15436450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138070397..138072296hg38UCSC Ensembl
Innerchr7:137755143..137757042hg19UCSC Ensembl
Innerchr7:137405683..137407582hg18UCSC Ensembl
Innerchr7:137212398..137214297hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381900
hg191900
hg181900
hg171900
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523950
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699798
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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