A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562363



Internal ID16349772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76036425..76088787hg38UCSC Ensembl
Innerchr13:76610561..76662923hg19UCSC Ensembl
Innerchr13:75508562..75560924hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3852363
hg1952363
hg1852363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv815785, nssv1176358
Samples1780854449_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562363
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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