A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467644



Internal ID245454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28050415..28054081hg38UCSC Ensembl
chr6:28018193..28021859hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383667
hg193667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv421n206
Supporting Variantsnssv16979399
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467644
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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