A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382331



Internal ID22287846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123253813..123256675hg38UCSC Ensembl
chr10:125013329..125016191hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382863
hg192863
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190543
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382331
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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