A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374659



Internal ID21032212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38143452..38149870hg38UCSC Ensembl
chr3:38184943..38191361hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386419
hg196419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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