A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352870



Internal ID22233082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98407737..98407796hg38UCSC Ensembl
chr10:100167494..100167553hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218458
Supporting Variants
SamplesHG00733
Known GenesPYROXD2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352870
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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