A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177437



Internal ID22334426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691332..68691625hg38UCSC Ensembl
chr15:68983671..68983964hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2970n152
Supporting Variantsnssv14430498, nssv14458660
SamplesHG00733, HG00514
Known GenesCORO2B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a AluY mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177437
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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