A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901164



Internal ID15848434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53419262..53507505hg38UCSC Ensembl
Innerchr19:53922515..54010759hg19UCSC Ensembl
Innerchr19:58614327..58702571hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3888244
hg1988245
hg1888245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580087
Supporting Variants
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901164
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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