A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561189



Internal ID16348598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18967770..19036868hg38UCSC Ensembl
Innerchr13:19541910..19611008hg19UCSC Ensembl
Innerchr13:18439910..18509008hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3869099
hg1969099
hg1869099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3069n54
Supporting Variantsnssv806025
Samples
Known GenesLINC00442
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561189
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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