A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676732



Internal ID15066698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94173569..94175706hg38UCSC Ensembl
Innerchr11:93906735..93908872hg19UCSC Ensembl
Innerchr11:93546383..93548520hg18UCSC Ensembl
Innerchr11:93546383..93548520hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382138
hg192138
hg182138
hg172138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517664
Supporting Variants
Samples
Known GenesPANX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676732
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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