A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14356413



Internal ID22210159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97405371..97405687hg38UCSC Ensembl
chr10:99165128..99165444hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214222
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14356413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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