A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562645



Internal ID16350054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89992703..90043001hg38UCSC Ensembl
Innerchr13:90644957..90695255hg19UCSC Ensembl
Innerchr13:89442958..89493256hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3850299
hg1950299
hg1850299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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