A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456565



Internal ID22250794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107654730..107654816hg38UCSC Ensembl
chr6:107975934..107976020hg19UCSC 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 Variantsnsv3183650
Supporting Variants
SamplesHG00733
Known GenesSOBP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456565
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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