A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14346071



Internal ID22117704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61213566..61215185hg38UCSC Ensembl
chr9:43605556..43607176hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg381620
hg191621
Variant TypeOTHER copy number variation
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197650
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14346071
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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