A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1448n209



Internal ID22827523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9996478..11875087hg38UCSC Ensembl
chr3:10038162..11916561hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381878610
hg191878400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5901270, nsv5891525, nsv5904127
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
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1448n209
Frequency
Sample Size914
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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