A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093086



Internal ID22002319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9901444..9901444hg38UCSC Ensembl
chr17:9804761..9804761hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617932
Samples
Known GenesRCVRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093086
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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