A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676715



Internal ID15413367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13268079..13903660hg38UCSC Ensembl
Innerchr21:14640400..15275981hg19UCSC Ensembl
Innerchr21:13562271..14197852hg18UCSC Ensembl
Innerchr21:13562271..14197852hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38635582
hg19635582
hg18635582
hg17635582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515654
Supporting Variants
Samples
Known GenesC21orf15, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676715
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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