A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553727



Internal ID16341136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22013323..22092022hg38UCSC Ensembl
Innerchr11:22034869..22113568hg19UCSC Ensembl
Innerchr11:21991445..22070144hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3878700
hg1978700
hg1878700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768865
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553727
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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