A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374903



Internal ID21032456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122772001..122801600hg38UCSC Ensembl
chr3:122490848..122520447hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3829600
hg1929600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4997n223
Supporting Variantsnssv18207952
Samples
Known GenesDIRC2, HSPBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374903
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