A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570637



Internal ID18868918
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 StatusS
Merged Variantsnsv1061876
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)nssv3570637
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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