A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061846



Internal ID18804377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19836118..20420512hg38UCSC Ensembl
Innerchr19:19946927..20603318hg19UCSC Ensembl
Innerchr19:19807927..20395158hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38584395
hg19656392
hg18587232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723295
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF253, ZNF486, ZNF682, ZNF826P, ZNF90, ZNF93
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061846
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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