A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519735



Internal ID15100342
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694344
Samples
Known GenesTEAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519735
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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