A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366768



Internal ID22592437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48355846..48978824hg38UCSC Ensembl
chr11:48377398..49000376hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38622979
hg19622979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976205
Supporting Variants
Samples
Known GenesOR4A47
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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