A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354584



Internal ID22176411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114010817..114014480hg38UCSC Ensembl
chr10:115770576..115774239hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383664
hg193664
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3236316
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354584
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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