A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060008



Internal ID18802539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20420512..20626420hg38UCSC Ensembl
Innerchr19:20603318..20809226hg19UCSC Ensembl
Innerchr19:20395158..20601066hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38205909
hg19205909
hg18205909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3465n100
Supporting Variantsnssv3569381
Samples
Known GenesZNF626, ZNF737, ZNF826P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060008
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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