A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461157



Internal ID239117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88498651..88498759hg38UCSC Ensembl
chr6:89208370..89208478hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986815
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461157
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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