A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469073



Internal ID246866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24883256..24886555hg38UCSC Ensembl
chr5:24883365..24886664hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469073
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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