A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065978



Internal ID19155197
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 StatusM
Merged Variantsdgv3585n100
Supporting Variantsnssv3723068
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)nsv1065978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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