A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698948



Internal ID15435600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41179214..41407805hg38UCSC Ensembl
Innerchr11:41200764..41429355hg19UCSC Ensembl
Innerchr11:41157340..41385931hg18UCSC Ensembl
Innerchr11:41157340..41385931hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38228592
hg19228592
hg18228592
hg17228592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523225
Supporting Variants
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698948
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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