A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349280



Internal ID22193342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133105101..133106500hg38UCSC Ensembl
chr9:135980488..135981887hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220753
Supporting Variants
SamplesHG00731
Known GenesRALGDS
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349280
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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