A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976205



Internal ID22751140
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 StatusM
Merged Variants
Supporting Variantsnssv17366768
Samples
Known GenesOR4A47
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976205
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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