A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562999



Internal ID16350408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105125866..105185548hg38UCSC Ensembl
Innerchr13:105778217..105837899hg19UCSC Ensembl
Innerchr13:104576218..104635900hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3859683
hg1959683
hg1859683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148929
Samples1780862085_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562999
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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