A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14400366



Internal ID22288973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35790336..35802531hg38UCSC Ensembl
chr6:35758113..35770308hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812196
hg1912196
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3178297
Supporting Variants
SamplesNA19240
Known GenesCLPS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14400366
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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