A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697020



Internal ID15433672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89915777..90080467hg38UCSC Ensembl
Innerchr7:89545091..89709781hg19UCSC Ensembl
Innerchr7:89383027..89547717hg18UCSC Ensembl
Innerchr7:89189742..89354432hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38164691
hg19164691
hg18164691
hg17164691
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697020
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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