A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004044



Internal ID21913387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25418033..25434955hg38UCSC Ensembl
chr6:25418261..25435183hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3816923
hg1916923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563320
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004044
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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