A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698641



Internal ID15435293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63081226..63105692hg38UCSC Ensembl
Innerchr11:62848698..62873164hg19UCSC Ensembl
Innerchr11:62605274..62629740hg18UCSC Ensembl
Innerchr11:62605274..62629740hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3824467
hg1924467
hg1824467
hg1724467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522971
Supporting Variants
Samples
Known GenesSLC22A24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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