A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463019



Internal ID240936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134491968..134493103hg38UCSC Ensembl
chr6:134813106..134814241hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969831
Samples
Known GenesLINC01010
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463019
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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