A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699356



Internal ID15089322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43443897..43453180hg38UCSC Ensembl
Innerchr21:44863777..44873060hg19UCSC Ensembl
Innerchr21:43688205..43697488hg18UCSC Ensembl
Innerchr21:43688205..43697488hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg389284
hg199284
hg189284
hg179284
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516339
Supporting Variants
Samples
Known GenesLINC00319
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699356
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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