A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467692



Internal ID245503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153182732..153207971hg38UCSC Ensembl
chr6:153503867..153529106hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3825240
hg1925240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467692
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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