A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv806055



Internal ID15753325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20218045..20456753hg38UCSC Ensembl
Innerchr13:20792184..21030892hg19UCSC Ensembl
Innerchr13:19690184..19928892hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38238709
hg19238709
hg18238709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561219
Supporting Variants
Samples
Known GenesCRYL1, GJB6, MIR4499
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv806055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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