A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551672



Internal ID325107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132944292..132944337hg38UCSC Ensembl
chr5:132279984..132280029hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974485
Samples
Known GenesAFF4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551672
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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