A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023476



Internal ID21932819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9255244..9264841hg38UCSC Ensembl
chr17:9158561..9168158hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg389598
hg199598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630255
Samples
Known GenesSTX8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023476
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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