A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201086



Internal ID22350441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:141638773..141685608hg38UCSC Ensembl
Outerchr4:142559926..142606761hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3846836
hg1946836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272754
SamplesHG00513
Known GenesIL15
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201086
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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