A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187341



Internal ID22339676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3322277..3325378hg38UCSC Ensembl
chr5:3322391..3325492hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7159n152
Supporting Variantsnssv14459265, nssv14457314
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)nsv3187341
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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