A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199711



Internal ID20766751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57546953..57547496hg38UCSC Ensembl
chr19:58058321..58058864hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520301
Supporting Variants
Samples
Known GenesZNF550
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199711
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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