A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179091



Internal ID22335358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61610588..61610638hg38UCSC Ensembl
chr5:60906415..60906465hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464859
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179091
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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