A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969076



Internal ID22744011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61096491..61144212hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3847722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444234
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969076
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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