A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580075



Internal ID16367484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53100337..53122859hg38UCSC Ensembl
Innerchr19:53603590..53626112hg19UCSC Ensembl
Innerchr19:58295402..58317924hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3822523
hg1922523
hg1822523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6533n54
Supporting Variantsnssv901154
Samples
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580075
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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