A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524067



Internal ID15104674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16020869..16039969hg38UCSC Ensembl
Innerchr19:16131679..16150779hg19UCSC Ensembl
Innerchr19:15992679..16011779hg18UCSC Ensembl
Innerchr19:15992679..16011779hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3819101
hg1919101
hg1819101
hg1719101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv200n21
Supporting Variantsnssv699935
Samples
Known GenesLINC00661, LINC00905
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524067
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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