A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199694



Internal ID22349246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63027042..63030333hg38UCSC Ensembl
chr20:61658394..61661685hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383292
hg193292
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14408557, nssv14408558
SamplesNA19240
Known GenesLOC63930
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199694
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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