A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562617



Internal ID16350026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86425798..86506854hg38UCSC Ensembl
Innerchr13:87078053..87159109hg19UCSC Ensembl
Innerchr13:85876054..85957110hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3881057
hg1981057
hg1881057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816728
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562617
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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