A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381731



Internal ID22287069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170086399..170088865hg38UCSC Ensembl
chr6:170401623..170404089hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382467
hg192467
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180043
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)nssv14381731
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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