A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376176



Internal ID21033729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142990498..143008015hg38UCSC Ensembl
chr4:143911651..143929168hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3817518
hg1917518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376176
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer