A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089597



Internal ID21998830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67565858..67565858hg38UCSC Ensembl
chr17:65561974..65561974hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627967
Samples
Known GenesPITPNC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089597
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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