A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698498



Internal ID15435150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:19998312..20002593hg38UCSC Ensembl
Innerchr11:20019858..20024139hg19UCSC Ensembl
Innerchr11:19976434..19980715hg18UCSC Ensembl
Innerchr11:19976434..19980715hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384282
hg194282
hg184282
hg174282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522845
Supporting Variants
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698498
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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