A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580082



Internal ID16367491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53369175..53445133hg38UCSC Ensembl
Innerchr19:53872428..53948386hg19UCSC Ensembl
Innerchr19:58564240..58640198hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3875959
hg1975959
hg1875959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150166
Samples1780846029_A
Known GenesTPM3P9, ZNF525, ZNF761, ZNF765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580082
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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