A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380905



Internal ID21038458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38733587..38734249hg38UCSC Ensembl
chr4:38735208..38735870hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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