A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414123



Internal ID21071676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103383529..103521548hg38UCSC Ensembl
chr5:102719230..102857249hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38138020
hg19138020
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414123
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