A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695519



Internal ID15432171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83739918..83751716hg38UCSC Ensembl
Innerchr7:83369234..83381032hg19UCSC Ensembl
Innerchr7:83207170..83218968hg18UCSC Ensembl
Innerchr7:83013885..83025683hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3811799
hg1911799
hg1811799
hg1711799
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518106
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695519
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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