A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459242



Internal ID22211784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704815..158704866hg38UCSC Ensembl
chr6:159125847..159125898hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179668
Supporting Variants
SamplesHG00733
Known GenesSYTL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459242
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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