A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515783



Internal ID15442840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34208970..34215745hg38UCSC Ensembl
Innerchr11:34230517..34237292hg19UCSC Ensembl
Innerchr11:34187093..34193868hg18UCSC Ensembl
Innerchr11:34187093..34193868hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386776
hg196776
hg186776
hg176776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664772, nssv659705, nssv677719, nssv674117, nssv671464
Samples
Known GenesABTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515783
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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