A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579601



Internal ID16367010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41500804..41525232hg38UCSC Ensembl
Innerchr19:42006714..42031592hg19UCSC Ensembl
Innerchr19:46698554..46723432hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3824429
hg1924879
hg1824879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899522
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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