A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220554



Internal ID22365215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999825..25999895hg38UCSC Ensembl
chr15:26244972..26245042hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2856n152
Supporting Variantsnssv14405745
SamplesNA19240
Known GenesLOC100128714
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220554
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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