A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086685



Internal ID21995918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41817471..41817471hg38UCSC Ensembl
chr17:39973723..39973723hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637008
Samples
Known GenesFKBP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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