A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699092



Internal ID15089058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37952931..37953928hg38UCSC Ensembl
Innerchr21:39325234..39326231hg19UCSC Ensembl
Innerchr21:38247104..38248101hg18UCSC Ensembl
Innerchr21:38247104..38248101hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
hg17998
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699092
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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