A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029585



Internal ID87419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136329928..136333424hg38UCSC Ensembl
chr9:139224384..139227881hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383497
hg193498
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555288
Supporting Variants
Samples
Known GenesGPSM1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029585
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010927


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