A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179668



Internal ID22335682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704815..158704866hg38UCSC Ensembl
chr6:159125847..159125898hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435718, nssv14459242
SamplesHG00733, HG00514
Known GenesSYTL3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179668
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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