A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579607



Internal ID16020330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41553480..41555814hg38UCSC Ensembl
Innerchr19:42059850..42062184hg19UCSC Ensembl
Innerchr19:46751690..46754024hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382335
hg192335
hg182335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6455n54
Supporting Variantsnssv899540
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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