A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060955



Internal ID20627995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33054836..33057775hg38UCSC Ensembl
chr1:33520437..33523376hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382940
hg192940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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