A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937482



Internal ID21357552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138952372..138952548hg38UCSC Ensembl
chr8:139964615..139964791hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15199436
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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