A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026691



Internal ID21936034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56792396..56793008hg38UCSC Ensembl
chr17:54869757..54870369hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624061
Samples
Known GenesC17orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026691
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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