A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461928



Internal ID239871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149930550..149949646hg38UCSC Ensembl
chr6:150251686..150270782hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3819097
hg1919097
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989650
Samples
Known GenesULBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461928
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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