A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437495



Internal ID22180564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168610191..168616759hg38UCSC Ensembl
chr6:169010871..169017439hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386569
hg196569
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3178699
Supporting Variants
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)nssv14437495
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer