A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182816



Internal ID22337299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2489643..2492408hg38UCSC Ensembl
chr5:2489757..2492522hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382766
hg192766
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7151n152
Supporting Variantsnssv14452842, nssv14460200
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)nsv3182816
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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