A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969272



Internal ID22744207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116715795..116716653hg38UCSC Ensembl
chr5:116051491..116052349hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424829
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969272
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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