A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17351966



Internal ID22577635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89706927..90017891hg38UCSC Ensembl
chr11:89440095..89751059hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38310965
hg19310965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976130
Supporting Variants
Samples
Known GenesMIR5692A1, TRIM49, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B, TRIM77
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17351966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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