A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046582



Internal ID20613622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36610902..36614412hg38UCSC Ensembl
chr19:37101804..37105314hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg383511
hg193511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531235
Supporting Variants
Samples
Known GenesZNF382
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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