A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516021



Internal ID15096628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5694619..5704342hg38UCSC Ensembl
Innerchr19:5694630..5704353hg19UCSC Ensembl
Innerchr19:5645630..5655353hg18UCSC Ensembl
Innerchr19:5645630..5655353hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389724
hg199724
hg189724
hg179724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665767, nssv681997
Samples
Known GenesLONP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516021
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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