A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712351



Internal ID136017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28373660..28378830hg38UCSC Ensembl
chr17:26700679..26705849hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385171
hg195171
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560784
Supporting Variants
Samples
Known GenesSARM1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712351
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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