A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580072



Internal ID16367481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53097592..53124524hg38UCSC Ensembl
Innerchr19:53600845..53627777hg19UCSC Ensembl
Innerchr19:58292657..58319589hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3826933
hg1926933
hg1826933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6533n54
Supporting Variantsnssv1150159
SamplesHGDP00214
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580072
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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