A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460618



Internal ID238594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139538136..139542425hg38UCSC Ensembl
chr5:138917721..138922010hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384290
hg194290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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