A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675467



Internal ID15065433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43302407hg38UCSC Ensembl
Innerchr19:43322065..43806559hg19UCSC Ensembl
Innerchr19:48013905..48498399hg18UCSC Ensembl
Innerchr19:48013905..48498399hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38484495
hg19484495
hg18484495
hg17484495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675467
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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