A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374651



Internal ID21032204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94060981..94061476hg38UCSC Ensembl
chr3:93779825..93780320hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106682
Samples
Known GenesDHFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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