A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658283



Internal ID15048249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43057570hg38UCSC Ensembl
Innerchr19:43374601..43561722hg19UCSC Ensembl
Innerchr19:48066441..48253562hg18UCSC Ensembl
Innerchr19:48066441..48253562hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38187122
hg19187122
hg18187122
hg17187122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG1, PSG11, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658283
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer