A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18083860



Internal ID20650900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191172889..191175284hg38UCSC Ensembl
chr2:192037615..192040010hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382396
hg192396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6342957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18083860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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