A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199686



Internal ID20766726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56669501..56672300hg38UCSC Ensembl
chr19:57180869..57183668hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527808
Supporting Variants
Samples
Known GenesZNF835
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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