A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5471143



Internal ID248887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135519327..135721578hg38UCSC Ensembl
chr6:135840465..136042716hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38202252
hg19202252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969862
Samples
Known GenesLINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5471143
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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