A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579368



Internal ID16366777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35170884..35189099hg38UCSC Ensembl
Innerchr19:35661787..35680002hg19UCSC Ensembl
Innerchr19:40353627..40371842hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3818216
hg1918216
hg1818216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898689
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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