A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908862



Internal ID6698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109281252..109281617hg38UCSC Ensembl
chr1:109823874..109824239hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432887
Supporting Variants
Samples
Known GenesPSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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