A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362469



Internal ID21020022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44984701..44998400hg38UCSC Ensembl
chr3:45026193..45039892hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209273
Samples
Known GenesEXOSC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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