A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200187



Internal ID20767227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53450080..53568103hg38UCSC Ensembl
chr19:53953334..54071357hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38118024
hg19118024
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518210
Supporting Variants
Samples
Known GenesZNF331, ZNF761, ZNF813
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200187
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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