A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485702



Internal ID263086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39449404..39454438hg38UCSC Ensembl
chr8:39306923..39311957hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg385035
hg195035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009603
Samples
Known GenesADAM3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485702
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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