A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197331



Internal ID20764371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11554378..11573447hg38UCSC Ensembl
chr19:11665193..11684262hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819070
hg1919070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521275
Supporting Variants
Samples
Known GenesELOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197331
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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