A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690042



Internal ID15080008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43155365hg38UCSC Ensembl
Innerchr19:43374601..43659517hg19UCSC Ensembl
Innerchr19:48066441..48351357hg18UCSC Ensembl
Innerchr19:48066441..48351357hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38284917
hg19284917
hg18284917
hg17284917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690042
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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