A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349272



Internal ID22285873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132883699..132884743hg38UCSC Ensembl
chr9:135759086..135760130hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381045
hg191045
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558728
Supporting Variants
SamplesNA19240
Known GenesC9orf9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349272
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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