A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553755



Internal ID16341164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23282087..23384959hg38UCSC Ensembl
Innerchr11:23303633..23406505hg19UCSC Ensembl
Innerchr11:23260209..23363081hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38102873
hg19102873
hg18102873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174748
SamplesNINDS_103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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