A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468562



Internal ID246356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90282733..90295047hg38UCSC Ensembl
chr6:90992452..91004766hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3812315
hg1912315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988324
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468562
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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