A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179985



Internal ID22335846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136430..35137031hg38UCSC Ensembl
chr6:35104207..35104808hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412234, nssv14457739, nssv14436971
SamplesNA19240, HG00733, HG00514
Known GenesTCP11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179985
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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