A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361213



Internal ID21018766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46845970..46851085hg38UCSC Ensembl
chr3:46887460..46892575hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385116
hg195116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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