A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3285778



Internal ID22384158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77077572..77077726hg38UCSC Ensembl
chr15:77369914..77370068hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2995n152
Supporting Variantsnssv14405361
SamplesNA19240
Known Genes
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)nsv3285778
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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