A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065516



Internal ID19154735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53426511..53510789hg38UCSC Ensembl
Innerchr19:53929764..54014043hg19UCSC Ensembl
Innerchr19:58621576..58705855hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3884279
hg1984280
hg1884280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n100
Supporting Variantsnssv3573261
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065516
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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