A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366798



Internal ID21024351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47883704..47885853hg38UCSC Ensembl
chr3:47925194..47927343hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100786
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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