A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970838



Internal ID22745773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149799559..149803857hg38UCSC Ensembl
chr3:149517346..149521644hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg384299
hg194299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415294
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970838
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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