A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591553



Internal ID20964624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119568183..123189997hg38UCSC Ensembl
chr11:119438894..123060705hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383621815
hg193621812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1324n223
Supporting Variantsnssv18223723
Samples
Known GenesARHGEF12, BLID, BSX, C11orf63, CLMP, CRTAM, GRIK4, HSPA8, LOC341056, LOC649133, MIR100, MIR100HG, MIR125B1, MIRLET7A2, OAF, POU2F3, PVRL1, SC5D, SORL1, TBCEL, TECTA, TMEM136, TRIM29, UBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591553
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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