A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178699



Internal ID22335155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168610191..168616759hg38UCSC Ensembl
chr6:169010871..169017439hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386569
hg196569
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8244n152
Supporting Variantsnssv14437495
SamplesHG00514
Known GenesSMOC2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178699
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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