A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901009



Internal ID1472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20080288..20084194hg38UCSC Ensembl
chr1:20406781..20410687hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383907
hg193907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428507
Supporting Variants
Samples
Known GenesPLA2G5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901009
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.012488


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