A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370904



Internal ID21028457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24446915..24454678hg38UCSC Ensembl
chr3:24488406..24496169hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg387764
hg197764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210440
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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