A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555449



Internal ID15996172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76990613..77021264hg38UCSC Ensembl
Innerchr11:76701657..76732308hg19UCSC Ensembl
Innerchr11:76379305..76409956hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3830652
hg1930652
hg1830652
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779223
Samples
Known GenesACER3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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