A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591356



Internal ID21783399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14662114..14662114hg38UCSC Ensembl
chr10:14704113..14704113hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094102
Supporting Variants
Samples
Known GenesFAM107B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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