A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652838



Internal ID15042804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43009507hg38UCSC Ensembl
Innerchr19:43374601..43513659hg19UCSC Ensembl
Innerchr19:48066441..48205499hg18UCSC Ensembl
Innerchr19:48066441..48205499hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38139059
hg19139059
hg18139059
hg17139059
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)nssv652838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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