A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424922



Internal ID22482792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151865496..151865784hg38UCSC Ensembl
chr5:151245057..151245345hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971803
Supporting Variants
Samples
Known GenesGLRA1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424922
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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