A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980002



Internal ID22754937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41729227..41730917hg38UCSC Ensembl
chr11:41750777..41752467hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381691
hg191691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349672
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980002
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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