A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332365



Internal ID22183525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13260121..13260280hg38UCSC Ensembl
chr10:13302121..13302280hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212831
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332365
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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