A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381082



Internal ID21038635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139033257..139042808hg38UCSC Ensembl
chr4:139954411..139963962hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg389552
hg199552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213030
Samples
Known GenesCCRN4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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