A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199671



Internal ID20766711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56237095..56257518hg38UCSC Ensembl
chr19:56748464..56768887hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3820424
hg1920424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527775
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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