A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14400486



Internal ID22326389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107654738..107654824hg38UCSC Ensembl
chr6:107975942..107976028hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172523
Supporting Variants
SamplesNA19240
Known GenesSOBP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14400486
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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