A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287386



Internal ID22385789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33907178..33907279hg38UCSC Ensembl
chr10:34196106..34196207hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv867n152
Supporting Variantsnssv14383521
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)nsv3287386
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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