A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697584



Internal ID15087550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77842592..78286890hg38UCSC Ensembl
Innerchr11:77553638..77997936hg19UCSC Ensembl
Innerchr11:77231286..77675584hg18UCSC Ensembl
Innerchr11:77231286..77675584hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38444299
hg19444299
hg18444299
hg17444299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520740
Supporting Variants
Samples
Known GenesAAMDC, ALG8, GAB2, INTS4, KCTD14, KCTD21, KCTD21-AS1, NDUFC2, NDUFC2-KCTD14, RNU6-83P, THRSP, USP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697584
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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