A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18048456



Internal ID20615496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:537409..539872hg38UCSC Ensembl
chr19:537409..539872hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382464
hg192464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529938
Supporting Variants
Samples
Known GenesCDC34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18048456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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