A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699247



Internal ID15089213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58786298..58864895hg38UCSC Ensembl
Innerchr11:58553771..58632368hg19UCSC Ensembl
Innerchr11:58310347..58388944hg18UCSC Ensembl
Innerchr11:58310347..58388944hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3878598
hg1978598
hg1878598
hg1778598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523481
Supporting Variants
Samples
Known GenesGLYATL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699247
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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