A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092750



Internal ID22001983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:85395315..85395315hg38UCSC Ensembl
chr13:85969450..85969450hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606372
Samples
Known GenesLINC00351
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092750
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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