A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386034



Internal ID21043587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110932101..110959100hg38UCSC Ensembl
chr4:111853257..111880256hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3827000
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209531
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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