A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389583



Internal ID21047136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112946101..113021000hg38UCSC Ensembl
chr4:113867257..113942156hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3874900
hg1974900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209559
Samples
Known GenesANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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