A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570636



Internal ID18868917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23438071..23888352hg38UCSC Ensembl
Innerchr19:23620873..24071154hg19UCSC Ensembl
Innerchr19:23412713..23862994hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38450282
hg19450282
hg18450282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059279
Supporting Variants
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)nssv3570636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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