A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198577



Internal ID20765617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4331888..4342037hg38UCSC Ensembl
chr19:4331885..4342034hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810150
hg1910150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528576
Supporting Variants
Samples
Known GenesSTAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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