A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668205



Internal ID15058171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43141405hg38UCSC Ensembl
Innerchr19:43322065..43645557hg19UCSC Ensembl
Innerchr19:48013905..48337397hg18UCSC Ensembl
Innerchr19:48013905..48337397hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38323493
hg19323493
hg18323493
hg17323493
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516973
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668205
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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