A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225324



Internal ID20792364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120551312..124267280hg38UCSC Ensembl
chr11:120422021..124137176hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383715969
hg193715156
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584901
Supporting Variants
Samples
Known GenesBLID, BSX, C11orf63, CLMP, CRTAM, GRAMD1B, GRIK4, HSPA8, LOC341056, MIR100, MIR100HG, MIR125B1, MIR4493, MIRLET7A2, OR10G4, OR10G7, OR10G8, OR10G9, OR10S1, OR4D5, OR6M1, OR6T1, OR6X1, OR8D4, OR8G1, OR8G2, OR8G5, SC5D, SCN3B, SORL1, TBCEL, TECTA, TMEM225, UBASH3B, VWA5A, ZNF202
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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