A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198110



Internal ID20765150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38819059..38819996hg38UCSC Ensembl
chr19:39309699..39310636hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524029
Supporting Variants
Samples
Known GenesECH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198110
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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