A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174576



Internal ID22332887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79842306..79852362hg38UCSC Ensembl
chr7:79471622..79481678hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3810057
hg1910057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380397
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)nsv3174576
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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