A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562631



Internal ID16350040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87726869..87817930hg38UCSC Ensembl
Innerchr13:88379124..88470185hg19UCSC Ensembl
Innerchr13:87177125..87268186hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3891062
hg1991062
hg1891062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816743
Samples
Known GenesLINC00397
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562631
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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