A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562561



Internal ID16349970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84397135..84688373hg38UCSC Ensembl
Innerchr13:84971270..85262508hg19UCSC Ensembl
Innerchr13:83869271..84160509hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38291239
hg19291239
hg18291239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816611
Samples
Known GenesLINC00333
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562561
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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