A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694367



Internal ID118033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90841764..90916508hg38UCSC Ensembl
chr13:91494018..91568762hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3874745
hg1974745
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561143
Supporting Variants
Samples
Known GenesLINC00410
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694367
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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