A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388454



Internal ID22315986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125228036..125228102hg38UCSC Ensembl
chr10:126916605..126916671hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205684
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)nssv14388454
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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