A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362785



Internal ID22588454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15856696..15881883hg38UCSC Ensembl
chr11:15878242..15903429hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3825188
hg1925188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362785
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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