A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704806



Internal ID15441458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37329883..37338729hg38UCSC Ensembl
Innerchr21:38702185..38711031hg19UCSC Ensembl
Innerchr21:37624055..37632901hg18UCSC Ensembl
Innerchr21:37624055..37632901hg17UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg388847
hg198847
hg188847
hg178847
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528244
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704806
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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