A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978494



Internal ID22753429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95916855..95917178hg38UCSC Ensembl
chr6:96364731..96365054hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438536
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978494
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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