A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095181



Internal ID22004414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68040236..68040236hg38UCSC Ensembl
chr17:66036352..66036352hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625845
Samples
Known GenesKPNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095181
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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