A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432978



Internal ID211707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109280158..109280393hg38UCSC Ensembl
chr1:109822780..109823015hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908859
Samples
Known GenesPSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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