A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456749



Internal ID234810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90112294..90113180hg38UCSC Ensembl
chr6:90822013..90822899hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38887
hg19887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985405
Samples
Known GenesBACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456749
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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