A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3556093



Internal ID22424927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35780243..35780243hg38UCSC Ensembl
chr10:36069171..36069171hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377891, nssv14414552, nssv14440269
SamplesNA19240, HG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3556093
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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