A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977848



Internal ID22752784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101375779..101571357hg38UCSC Ensembl
chr11:101246510..101442088hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38195579
hg19195579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368848
Samples
Known GenesMIR3920, TRPC6
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977848
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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