A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052387



Internal ID20619427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152986701..152990200hg38UCSC Ensembl
chr1:152959177..152962676hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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