A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592460



Internal ID21784503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59308597..59308597hg38UCSC Ensembl
chr10:61068357..61068357hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6096920
Supporting Variants
Samples
Known GenesFAM13C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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