A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473007



Internal ID250707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106663186..106665778hg38UCSC Ensembl
chr6:107111061..107113653hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382593
hg192593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986307
Samples
Known GenesQRSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473007
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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