A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222590



Internal ID22366622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68257829..68257889hg38UCSC Ensembl
chr15:68550167..68550227hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2968n152
Supporting Variantsnssv14430494, nssv14463079
SamplesHG00733, 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)nsv3222590
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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