A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989650



Internal ID60522
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 StatusS
Merged Variantsnsv5461928
Supporting Variants
Samples
Known GenesULBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989650
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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