A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659705



Internal ID15396357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34208970..34212598hg38UCSC Ensembl
Innerchr11:34230517..34234145hg19UCSC Ensembl
Innerchr11:34187093..34190721hg18UCSC Ensembl
Innerchr11:34187093..34190721hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383629
hg193629
hg183629
hg173629
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515783
Supporting Variants
Samples
Known GenesABTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659705
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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