A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714944



Internal ID138610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79739886..79741196hg38UCSC Ensembl
chr17:77713685..77714995hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555573
Supporting Variants
Samples
Known GenesENPP7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714944
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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