A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227990



Internal ID22370313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:39032681..39184710hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38152030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv886n152
Supporting Variantsnssv14437712
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)nsv3227990
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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