A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089158



Internal ID20656198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62384701..62387900hg38UCSC Ensembl
chr2:62611836..62615035hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343462
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00077


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