A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764536



Internal ID16058492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2428546..2429867hg38UCSC Ensembl
Innerchr11:2449776..2451097hg19UCSC Ensembl
Innerchr11:2406352..2407673hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381322
hg191322
hg181322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553106
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764536
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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