A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071343



Internal ID21980576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131357263..131357263hg38UCSC Ensembl
chr3:131076107..131076107hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549636
Samples
Known GenesLOC339874
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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