A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579610



Internal ID16020333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41554997..41555707hg38UCSC Ensembl
Innerchr19:42061367..42062077hg19UCSC Ensembl
Innerchr19:46753207..46753917hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38711
hg19711
hg18711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6456n54
Supporting Variantsnssv899543, nssv899545, nssv899544
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579610
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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