A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14454588



Internal ID22249158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32663171..32663262hg38UCSC Ensembl
chr6:32630948..32631039hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185733
Supporting Variants
SamplesHG00733
Known GenesHLA-DQB1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14454588
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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