A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062574



Internal ID21971807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144824437..144824437hg38UCSC Ensembl
chr6:145145573..145145573hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576694
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062574
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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