A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778988



Internal ID15726258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72233198..72238908hg38UCSC Ensembl
Innerchr11:71944242..71949952hg19UCSC Ensembl
Innerchr11:71621890..71627600hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385711
hg195711
hg185711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555404
Supporting Variants
Samples
Known GenesINPPL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778988
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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