A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582071



Internal ID21774114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6229149..6229149hg38UCSC Ensembl
chr10:6271112..6271112hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097028
Supporting Variants
Samples
Known GenesPFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582071
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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