A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457248



Internal ID235297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90877899..90881377hg38UCSC Ensembl
chr6:91587617..91591095hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg383479
hg193479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457248
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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