A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355201



Internal ID22267668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123619425..123619498hg38UCSC Ensembl
chr10:125378941..125379014hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527921
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355201
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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