A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555153



Internal ID15995876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60996360..61044985hg38UCSC Ensembl
Innerchr11:60763832..60812457hg19UCSC Ensembl
Innerchr11:60520408..60569033hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3848626
hg1948626
hg1848626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174802
SamplesHGDP00774
Known GenesCD6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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