A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18077285



Internal ID20644325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:142312858..142313330hg38UCSC Ensembl
chr2:143070427..143070899hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18077285
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00101


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