A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089160



Internal ID20656200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62435301..62443100hg38UCSC Ensembl
chr2:62662436..62670235hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089160
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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