A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14390741



Internal ID22292748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132191848..132191902hg38UCSC Ensembl
chr10:134005352..134005406hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195174
Supporting Variants
SamplesNA19240
Known GenesDPYSL4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14390741
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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