A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723068



Internal ID19021349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43085287..43252073hg38UCSC Ensembl
Innerchr19:43589439..43756225hg19UCSC Ensembl
Innerchr19:48281279..48448065hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38166787
hg19166787
hg18166787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065978
Supporting Variants
Samples
Known GenesLOC284344, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3723068
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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