A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18075907



Internal ID20642947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:120090227..120090897hg38UCSC Ensembl
chr2:120847803..120848473hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355053
Supporting Variants
Samples
Known GenesEPB41L5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18075907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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