A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052448



Internal ID20619488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160235251..160235782hg38UCSC Ensembl
chr1:160205041..160205572hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323736
Supporting Variants
Samples
Known GenesDCAF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00539


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