A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902387



Internal ID2397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24751528..24756213hg38UCSC Ensembl
chr1:25078019..25082704hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg384686
hg194686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417026
Supporting Variants
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902387
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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