A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526372



Internal ID15106979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:49853907..49877601hg38UCSC Ensembl
Innerchr19:50357164..50380858hg19UCSC Ensembl
Innerchr19:55048976..55072670hg18UCSC Ensembl
Innerchr19:55048976..55072670hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3823695
hg1923695
hg1823695
hg1723695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702668
Samples
Known GenesAKT1S1, MIR4749, PNKP, PTOV1, TBC1D17
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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