A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579049



Internal ID16366458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23489124..23878342hg38UCSC Ensembl
Innerchr19:23671926..24061144hg19UCSC Ensembl
Innerchr19:23463766..23852984hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38389219
hg19389219
hg18389219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6344n54
Supporting Variantsnssv896912
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)nsv579049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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