A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580076



Internal ID16367485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53100337..53123260hg38UCSC Ensembl
Innerchr19:53603590..53626513hg19UCSC Ensembl
Innerchr19:58295402..58318325hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3822924
hg1922924
hg1822924
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6533n54
Supporting Variantsnssv901155
Samples
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580076
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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