A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714686



Internal ID138352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76098358..76110794hg38UCSC Ensembl
chr17:74094439..74106875hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3812437
hg1912437
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5515588
Supporting Variants
Samples
Known GenesEXOC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714686
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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