A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556461



Internal ID15997184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117726212..117758753hg38UCSC Ensembl
Innerchr11:117596927..117629468hg19UCSC Ensembl
Innerchr11:117102137..117134678hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832542
hg1932542
hg1832542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784608
Samples
Known GenesDSCAML1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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