A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457908



Internal ID235943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89774900..89774966hg38UCSC Ensembl
chr6:90484619..90484685hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985379
Samples
Known GenesMDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457908
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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