A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14400491



Internal ID22326415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110031681..110031773hg38UCSC Ensembl
chr6:110352884..110352976hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185793
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)nssv14400491
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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