A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675144



Internal ID15411796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56902354..56923738hg38UCSC Ensembl
Innerchr11:56669830..56691213hg19UCSC Ensembl
Innerchr11:56426406..56447789hg18UCSC Ensembl
Innerchr11:56426406..56447789hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3821385
hg1921384
hg1821384
hg1721384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520375
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675144
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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