A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083852



Internal ID20650892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190939201..190940600hg38UCSC Ensembl
chr2:191803927..191805326hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345730
Supporting Variants
Samples
Known GenesGLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083852
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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