A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694344



Internal ID15084310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12817962..12843894hg38UCSC Ensembl
Innerchr11:12839509..12865441hg19UCSC Ensembl
Innerchr11:12796085..12822017hg18UCSC Ensembl
Innerchr11:12796085..12822017hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3825933
hg1925933
hg1825933
hg1725933
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519735
Supporting Variants
Samples
Known GenesTEAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694344
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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