A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064890



Internal ID20631930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88907483..88930351hg38UCSC Ensembl
chr1:89373166..89396034hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3822869
hg1922869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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