A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176294



Internal ID22333797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1858408..1858459hg38UCSC Ensembl
chr5:1858522..1858573hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14411756
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176294
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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