A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694265



Internal ID15430917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129811015..129811104hg38UCSC Ensembl
Innerchr7:129450855..129450944hg19UCSC Ensembl
Innerchr7:129238091..129238180hg18UCSC Ensembl
Innerchr7:129044806..129044895hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3890
hg1990
hg1890
hg1790
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518710
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694265
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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