A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182978



Internal ID22337383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149648568..149652541hg38UCSC Ensembl
chr5:149028131..149032104hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7560n152
Supporting Variantsnssv14436858, nssv14436859
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182978
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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