A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354846



Internal ID22141462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85822809..85882394hg38UCSC Ensembl
chr10:87582566..87642151hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3859586
hg1959586
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3216338
Supporting Variants
SamplesHG00513
Known GenesGRID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354846
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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