A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461012



Internal ID238977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21497884..21498001hg38UCSC Ensembl
chr6:21498115..21498232hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982224
Samples
Known GenesLINC00581
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461012
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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