A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066291



Internal ID19155510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53435068..53508635hg38UCSC Ensembl
Innerchr19:53938321..54011889hg19UCSC Ensembl
Innerchr19:58630133..58703701hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3873568
hg1973569
hg1873569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n100
Supporting Variantsnssv3573270
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)nsv1066291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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