A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703319



Internal ID15093285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43443897..43450270hg38UCSC Ensembl
Innerchr21:44863777..44870150hg19UCSC Ensembl
Innerchr21:43688205..43694578hg18UCSC Ensembl
Innerchr21:43688205..43694578hg17UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg386374
hg196374
hg186374
hg176374
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)nssv703319
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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