A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459864



Internal ID237870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:148319200..148327659hg38UCSC Ensembl
chr5:147698763..147707222hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg388460
hg198460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975614
Samples
Known GenesLOC102546294
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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