A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470238



Internal ID248008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115182060..115196455hg38UCSC Ensembl
chr5:114517757..114532152hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3814396
hg1914396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470238
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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