A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743065



Internal ID20519051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9994574..11870474hg38UCSC Ensembl
chr3:10036258..11911948hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381875901
hg191875691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv58n199
Supporting Variantsnssv16283778
Samples
Known GenesATG7, ATP2B2, BRK1, CIDECP, EMC3-AS1, FANCD2, FANCD2OS, GHRL, GHRLOS, HRH1, IRAK2, LINC00606, LINC00852, LOC401052, MIR885, SEC13, SLC6A1, SLC6A11, SLC6A1-AS1, TAMM41, TATDN2, VGLL4, VHL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743065
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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