A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18087860



Internal ID20654900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41944201..41949500hg38UCSC Ensembl
chr2:42171341..42176640hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337460
Supporting Variants
Samples
Known GenesC2orf91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18087860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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