A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061051



Internal ID19150270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53425499..53499258hg38UCSC Ensembl
Innerchr19:53928752..54002512hg19UCSC Ensembl
Innerchr19:58620564..58694324hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3873760
hg1973761
hg1873761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n100
Supporting Variantsnssv3573249
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)nsv1061051
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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