A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14405339



Internal ID22286830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68860123..68860300hg38UCSC Ensembl
chr15:69152462..69152639hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3285919
Supporting Variants
SamplesNA19240
Known GenesMIR548H4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14405339
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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