A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668921



Internal ID15058887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42817913..43057570hg38UCSC Ensembl
Innerchr19:43322065..43561722hg19UCSC Ensembl
Innerchr19:48013905..48253562hg18UCSC Ensembl
Innerchr19:48013905..48253562hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38239658
hg19239658
hg18239658
hg17239658
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, PSG6, PSG7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668921
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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