A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347162



Internal ID22145961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38646501..38646689hg38UCSC Ensembl
chr9:38646498..38646686hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529098
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347162
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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