A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561591



Internal ID16002314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48560276..48595434hg38UCSC Ensembl
Innerchr13:49134412..49169570hg19UCSC Ensembl
Innerchr13:48032413..48067571hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3835159
hg1935159
hg1835159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175939
SamplesNINDS_163
Known GenesLINC00462
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561591
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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