A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688324



Internal ID15078290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117233820..117280696hg38UCSC Ensembl
Innerchr11:117104536..117151412hg19UCSC Ensembl
Innerchr11:116609746..116656622hg18UCSC Ensembl
Innerchr11:116609746..116656622hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3846877
hg1946877
hg1846877
hg1746877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516483
Supporting Variants
Samples
Known GenesRNF214
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688324
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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