A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978918



Internal ID22753853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148641915..148651218hg38UCSC Ensembl
chr6:148963051..148972354hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg389304
hg199304
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412857
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978918
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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