A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065584



Internal ID19154803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52539873..52624206hg38UCSC Ensembl
Innerchr19:53043126..53127459hg19UCSC Ensembl
Innerchr19:57734938..57819271hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3884334
hg1984334
hg1884334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3572061
Samples
Known GenesZNF137P, ZNF701, ZNF808, ZNF83
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065584
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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