A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047157



Internal ID20614197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49387868..49388572hg38UCSC Ensembl
chr19:49891125..49891829hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38705
hg19705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529622
Supporting Variants
Samples
Known GenesCCDC155
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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