A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073539



Internal ID21982772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157039670..157039670hg38UCSC Ensembl
chr6:157360804..157360804hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565574
Samples
Known GenesARID1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073539
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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