A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519718



Internal ID15447011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34620946..34759389hg38UCSC Ensembl
Innerchr11:34642493..34780936hg19UCSC Ensembl
Innerchr11:34599069..34737512hg18UCSC Ensembl
Innerchr11:34599069..34737512hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38138444
hg19138444
hg18138444
hg17138444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv63n21
Supporting Variantsnssv697010
Samples
Known GenesEHF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519718
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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