A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094991



Internal ID22004224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30806775..30806775hg38UCSC Ensembl
chr13:31380912..31380912hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610738
Samples
Known GenesLINC00398
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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