A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380291



Internal ID21037844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46692801..46734300hg38UCSC Ensembl
chr4:46694818..46736317hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3841500
hg1941500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5257n223
Supporting Variantsnssv18213706
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380291
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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