A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047621



Internal ID20614661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31791601..31794200hg38UCSC Ensembl
chr19:32282507..32285106hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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