A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190103



Internal ID22341096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164327534..164330285hg38UCSC Ensembl
chr5:163754540..163757291hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436900
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)nsv3190103
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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