A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047674



Internal ID20614714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32710690..32717127hg38UCSC Ensembl
chr19:33201596..33208033hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386438
hg196438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516710
Supporting Variants
Samples
Known GenesNUDT19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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