A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346105



Internal ID22117832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63253494..63413073hg38UCSC Ensembl
chr9:67208466..67366296hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38159580
hg19157831
Variant TypeCNV duplication
Copy Number17
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224420
Supporting Variants
SamplesHG00512
Known GenesAQP7P1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346105
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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