A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714746



Internal ID138412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76761450..76761501hg38UCSC Ensembl
chr17:74757532..74757583hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538886
Supporting Variants
Samples
Known GenesMFSD11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714746
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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