A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381689



Internal ID21039242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41855101..41886600hg38UCSC Ensembl
chr4:41857118..41888617hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3831500
hg1931500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213639
Samples
Known GenesLINC00682
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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