A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561335



Internal ID16002058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23393551..23422058hg38UCSC Ensembl
Innerchr13:23967690..23996197hg19UCSC Ensembl
Innerchr13:22865690..22894197hg18UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg3828508
hg1928508
hg1828508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806765
Samples
Known GenesSACS, SACS-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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