A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890021



Internal ID167476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:145181587..145210793hg38UCSC Ensembl
chr1:144312987..144335677hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3829207
hg1922691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426710
Supporting Variants
Samples
Known GenesLINC00623, LOC100288142, LOC728875
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000472


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