A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479824



Internal ID257340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38868370..38872364hg38UCSC Ensembl
chr8:38725888..38729882hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg383995
hg193995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009555
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479824
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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