A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046299



Internal ID20613339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35616394..35619635hg38UCSC Ensembl
chr19:36107296..36110537hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383242
hg193242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518836
Supporting Variants
Samples
Known GenesHAUS5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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