A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714777



Internal ID138443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77469889..77469967hg38UCSC Ensembl
chr17:75465971..75466049hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528924
Supporting Variants
Samples
Known GenesSEPT9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714777
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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