A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031198



Internal ID88501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134885391..134913028hg38UCSC Ensembl
chr9:137777237..137804874hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3827638
hg1927638
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558903
Supporting Variants
Samples
Known GenesFCN1, FCN2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031198
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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