A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048720



Internal ID20615760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51484508..51486127hg38UCSC Ensembl
chr19:51987762..51989381hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520450
Supporting Variants
Samples
Known GenesCEACAM18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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