A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680394



Internal ID15070360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43057570..43302843hg38UCSC Ensembl
Innerchr19:43561722..43806995hg19UCSC Ensembl
Innerchr19:48253562..48498835hg18UCSC Ensembl
Innerchr19:48253562..48498835hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38245274
hg19245274
hg18245274
hg17245274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680394
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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