A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979006



Internal ID22753941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155085430..155087645hg38UCSC Ensembl
chr5:154464990..154467205hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382216
hg192216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414750
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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