A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14399508



Internal ID22286866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14523506..14525943hg38UCSC Ensembl
chr6:14523737..14526174hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382438
hg192438
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180351
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)nssv14399508
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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