A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352871



Internal ID22280589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98419103..98419474hg38UCSC Ensembl
chr10:100178860..100179231hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3215352
Supporting Variants
SamplesNA19239
Known GenesHPS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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