A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561243



Internal ID16001966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20980645..21091500hg38UCSC Ensembl
Innerchr13:21554784..21665639hg19UCSC Ensembl
Innerchr13:20452784..20563639hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38110856
hg19110856
hg18110856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806153
Samples
Known GenesLATS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561243
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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