A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347592



Internal ID22293882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70385158..70386361hg38UCSC Ensembl
chr9:73000074..73001277hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381204
hg191204
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218616
Supporting Variants
SamplesNA19240
Known GenesKLF9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347592
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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