A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660336



Internal ID15396988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13268079..13656214hg38UCSC Ensembl
Innerchr21:14640400..15028535hg19UCSC Ensembl
Innerchr21:13562271..13950406hg18UCSC Ensembl
Innerchr21:13562271..13950406hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38388136
hg19388136
hg18388136
hg17388136
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515654
Supporting Variants
Samples
Known GenesLOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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