A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361743



Internal ID22587412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160235187..160235791hg38UCSC Ensembl
chr1:160204977..160205581hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881764
Supporting Variants
Samples
Known GenesDCAF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361743
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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