A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14336737



Internal ID22253400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23790542..23790673hg38UCSC Ensembl
chr10:24079471..24079602hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224010
Supporting Variants
SamplesNA19238
Known GenesKIAA1217
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14336737
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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