A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213007



Internal ID22360090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128395662..128395849hg38UCSC Ensembl
chr9:131157941..131158128hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348435, nssv14348436
SamplesNA19239, HG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213007
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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