A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021570



Internal ID21930913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8963463..9103085hg38UCSC Ensembl
chr17:8866780..9006402hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38139623
hg19139623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623804
Samples
Known GenesNTN1, PIK3R5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021570
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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