A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181187



Internal ID22336449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132302587..132302737hg38UCSC Ensembl
chr5:131638280..131638430hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399860
SamplesNA19240
Known GenesSLC22A4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3181187
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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