A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466428



Internal ID244267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132314608..132314686hg38UCSC Ensembl
chr6:132635747..132635825hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970056
Samples
Known GenesMOXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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