A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077299



Internal ID20644339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142551301..142556600hg38UCSC Ensembl
chr2:143308870..143314169hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6336990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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