A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16893148



Internal ID169589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183613547..183619229hg38UCSC Ensembl
chr1:183582682..183588364hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385683
hg195683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16893148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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