A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061876



Internal ID19151095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23438738..23888352hg38UCSC Ensembl
Innerchr19:23621540..24071154hg19UCSC Ensembl
Innerchr19:23413380..23862994hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38449615
hg19449615
hg18449615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3479n100
Supporting Variantsnssv3570637
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061876
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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