A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561711



Internal ID16349120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55742350..55830115hg38UCSC Ensembl
Innerchr13:56316484..56404249hg19UCSC Ensembl
Innerchr13:55214485..55302250hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3887766
hg1987766
hg1887766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176354
SamplesNINDS_2
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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