A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347857



Internal ID22188815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85454683..85454743hg38UCSC Ensembl
chr9:88069598..88069658hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529402
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347857
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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