A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18056183



Internal ID20623224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:197968310..197968724hg38UCSC Ensembl
chr1:197937440..197937854hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18056183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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