A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172474



Internal ID22331825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108952564..108952622hg38UCSC Ensembl
chr5:108288265..108288323hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461777
SamplesHG00733
Known GenesFER
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3172474
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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