A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048547



Internal ID20615587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57120107..57121246hg38UCSC Ensembl
chr19:57631475..57632614hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529047
Supporting Variants
Samples
Known GenesUSP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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