A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976562



Internal ID22751497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151859161..151861846hg38UCSC Ensembl
chr5:151238722..151241407hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382686
hg192686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425105
Samples
Known GenesGLRA1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976562
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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