A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1324n223



Internal ID22804292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119568183..124267280hg38UCSC Ensembl
chr11:119438894..124137176hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384699098
hg194698283
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6584901, nsv6591553
Samples
Known GenesARHGEF12, BLID, BSX, C11orf63, CLMP, CRTAM, GRAMD1B, GRIK4, HSPA8, LOC341056, LOC649133, MIR100, MIR100HG, MIR125B1, MIR4493, MIRLET7A2, OAF, OR10G4, OR10G7, OR10G8, OR10G9, OR10S1, OR4D5, OR6M1, OR6T1, OR6X1, OR8D4, OR8G1, OR8G2, OR8G5, POU2F3, PVRL1, SC5D, SCN3B, SORL1, TBCEL, TECTA, TMEM136, TMEM225, TRIM29, UBASH3B, VWA5A, ZNF202
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1324n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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