A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556582



Internal ID15997305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132056304..132060294hg38UCSC Ensembl
Innerchr11:131926198..131930188hg19UCSC Ensembl
Innerchr11:131431408..131435398hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383991
hg193991
hg183991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2201n54
Supporting Variantsnssv785124, nssv785125
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556582
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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