A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355437



Internal ID22581106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154749878..154749956hg38UCSC Ensembl
chr1:154722354..154722432hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872570
Supporting Variants
Samples
Known GenesKCNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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