A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529098



Internal ID22398491
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347163, nssv14347165, nssv14347161, nssv14347164, nssv14347162
SamplesNA19238, HG00732, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529098
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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