A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14449588



Internal ID22244877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6852996..6853047hg38UCSC Ensembl
chrUn_gl000215:62339..62390hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200620
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)nssv14449588
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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