A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18058843



Internal ID20625883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235163580..235165409hg38UCSC Ensembl
chr1:235326895..235328724hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg381830
hg191830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18058843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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