A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906922



Internal ID22682126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25363095..25363258hg38UCSC Ensembl
chr6:25363323..25363486hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436296
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906922
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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