A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460315



Internal ID22212873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153304429..153304664hg38UCSC Ensembl
chr6:153625564..153625799hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3186186
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460315
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