A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901682



Internal ID15848952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54755316..54758026hg38UCSC Ensembl
Innerchr19:55266768..55269478hg19UCSC Ensembl
Innerchr19:59958580..59961290hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382711
hg192711
hg182711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580271
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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