A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3181761



Internal ID22336743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133624788..133627265hg38UCSC Ensembl
chr5:132960479..132962956hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382478
hg192478
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7528n152
Supporting Variantsnssv14436834, nssv14436833
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)nsv3181761
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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