A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215399



Internal ID22361747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124876603..124876793hg38UCSC Ensembl
chr10:126565172..126565362hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1092n152
Supporting Variantsnssv14412802
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)nsv3215399
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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