A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14425763



Internal ID22165819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19730548..19730613hg38UCSC Ensembl
chr6:19730779..19730844hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186814
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14425763
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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