A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352319



Internal ID22208165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69083412..69083909hg38UCSC Ensembl
chr10:70843168..70843665hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221289
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352319
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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