A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080103



Internal ID20647143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186353246..186356529hg38UCSC Ensembl
chr2:187217973..187221256hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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