A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580008



Internal ID16367417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52305733..52362918hg38UCSC Ensembl
Innerchr19:52808986..52866171hg19UCSC Ensembl
Innerchr19:57500798..57557983hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3857186
hg1957186
hg1857186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150143
SamplesHGDP01189
Known GenesZNF480, ZNF610
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580008
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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