A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14257907



Internal ID22275122
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226514
Supporting Variants
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)nssv14257907
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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