A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367150



Internal ID21024703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9876605..9881289hg38UCSC Ensembl
chr3:9918289..9922973hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384685
hg194685
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211296
Samples
Known GenesCIDEC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367150
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