A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467484



Internal ID245296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103491627..103495345hg38UCSC Ensembl
chr6:103939502..103943220hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg383719
hg193719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467484
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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