A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065193



Internal ID20632233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92572526..92576164hg38UCSC Ensembl
chr1:93038083..93041721hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg383639
hg193639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332780
Supporting Variants
Samples
Known GenesEVI5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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