A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17050700



Internal ID101678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107764907..107928505hg38UCSC Ensembl
chr11:107635633..107799231hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38163599
hg19163599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143015
Supporting Variants
Samples
Known GenesSLC35F2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17050700
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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