A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355137



Internal ID22127684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121634838..121635531hg38UCSC Ensembl
chr10:123394352..123395045hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227502
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355137
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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