A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660399



Internal ID15397051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13268079..13843493hg38UCSC Ensembl
Innerchr21:14640400..15215814hg19UCSC Ensembl
Innerchr21:13562271..14137685hg18UCSC Ensembl
Innerchr21:13562271..14137685hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38575415
hg19575415
hg18575415
hg17575415
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)nssv660399
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer