A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484537



Internal ID261947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132161707..132161794hg38UCSC Ensembl
chr7:131846466..131846553hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17006190
Samples
Known GenesPLXNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484537
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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