A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179484



Internal ID22335583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35789939..35802146hg38UCSC Ensembl
chr6:35757716..35769923hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3812208
hg1912208
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7856n152
Supporting Variantsnssv14426429
SamplesHG00514
Known GenesCLPS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179484
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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