A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376036



Internal ID21033589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67893901..67899800hg38UCSC Ensembl
chr4:68759619..68765518hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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