A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096521



Internal ID22005754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24633403..24633403hg38UCSC Ensembl
chr14:25102609..25102609hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604103
Samples
Known GenesGZMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096521
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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