A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14411456



Internal ID22310302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815436..4815656hg38UCSC Ensembl
chr10:4857628..4857848hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3285089
Supporting Variants
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)nssv14411456
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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