A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580045



Internal ID16020768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52871534..52898507hg38UCSC Ensembl
Innerchr19:53374787..53401760hg19UCSC Ensembl
Innerchr19:58066599..58093572hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3826974
hg1926974
hg1826974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901099
Samples
Known GenesZNF320
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580045
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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