A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346980



Internal ID22185300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77570919..77571038hg38UCSC Ensembl
chr9:80185835..80185954hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217629
Supporting Variants
SamplesHG00731
Known GenesGNA14
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346980
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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