A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049482



Internal ID20616522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57663193..57716324hg38UCSC Ensembl
chr19:58174561..58227692hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3853132
hg1953132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529426
Supporting Variants
Samples
Known GenesZNF154, ZNF551, ZSCAN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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