A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579614



Internal ID16020337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41555059..41555814hg38UCSC Ensembl
Innerchr19:42061429..42062184hg19UCSC Ensembl
Innerchr19:46753269..46754024hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38756
hg19756
hg18756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6456n54
Supporting Variantsnssv899561
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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