A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374328



Internal ID21031881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155761843..155795690hg38UCSC Ensembl
chr3:155479632..155513479hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3833848
hg1933848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209746
Samples
Known GenesC3orf33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374328
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