A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882380



Internal ID22657357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109424945..109425035hg38UCSC Ensembl
chr1:109967567..109967657hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353076
Samples
Known GenesPSMA5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882380
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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