A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465622



Internal ID243481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107626666..107781739hg38UCSC Ensembl
chr4:108547822..108702895hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38155074
hg19155074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954816
Samples
Known GenesPAPSS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465622
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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