A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047672



Internal ID20614712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32695295..32704285hg38UCSC Ensembl
chr19:33186201..33195191hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg388991
hg198991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519232
Supporting Variants
Samples
Known GenesNUDT19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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