A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083525



Internal ID21992758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131367440..131367440hg38UCSC Ensembl
chr12:131851985..131851985hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609366
Samples
Known GenesLOC338797
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083525
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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