A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579047



Internal ID16366456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23437830..23886641hg38UCSC Ensembl
Innerchr19:23620632..24069443hg19UCSC Ensembl
Innerchr19:23412472..23861283hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38448812
hg19448812
hg18448812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6344n54
Supporting Variantsnssv896909, nssv896910
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579047
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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