A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226514



Internal ID22369290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28400926..28506689hg38UCSC Ensembl
Outerchr15:28646072..28751835hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38105764
hg19105764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14257907
SamplesNA19239
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226514
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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