A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556581



Internal ID15997304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131743728..131779552hg38UCSC Ensembl
Innerchr11:131613622..131649446hg19UCSC Ensembl
Innerchr11:131118832..131154656hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3835825
hg1935825
hg1835825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176204
Samples1780854295_A
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556581
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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