A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14457739



Internal ID22251739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136430..35137031hg38UCSC Ensembl
chr6:35104207..35104808hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179985
Supporting Variants
SamplesHG00733
Known GenesTCP11
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14457739
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