A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556637



Internal ID16344046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134864402hg38UCSC Ensembl
Innerchr11:134349754..134734296hg19UCSC Ensembl
Innerchr11:133854964..134239506hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38384543
hg19384543
hg18384543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv785180, nssv1176223
Samples1780854467_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556637
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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