A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347873



Internal ID22188876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134135131..134137027hg38UCSC Ensembl
chr9:137000253..137002149hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381897
hg191897
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226091
Supporting Variants
SamplesHG00731
Known GenesWDR5
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347873
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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