A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521656



Internal ID15102263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5704342..5711206hg38UCSC Ensembl
Innerchr19:5704353..5711217hg19UCSC Ensembl
Innerchr19:5655353..5662217hg18UCSC Ensembl
Innerchr19:5655353..5662217hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386865
hg196865
hg186865
hg176865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698274
Samples
Known GenesLONP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521656
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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