A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200620



Internal ID22350040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6852996..6853047hg38UCSC Ensembl
chrUn_gl000215:62339..62390hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14449588
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)nsv3200620
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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