A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700618



Internal ID15090584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:121070874..121084060hg38UCSC Ensembl
Innerchr11:120941583..120954769hg19UCSC Ensembl
Innerchr11:120446793..120459979hg18UCSC Ensembl
Innerchr11:120446793..120459979hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3813187
hg1913187
hg1813187
hg1713187
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524651
Supporting Variants
Samples
Known GenesTBCEL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700618
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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