A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554019



Internal ID16341428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37804340..37874114hg38UCSC Ensembl
Innerchr11:37825890..37895664hg19UCSC Ensembl
Innerchr11:37782466..37852240hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3869775
hg1969775
hg1869775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174620
Samples1780862042_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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