A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976738



Internal ID22751673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8779905..8818869hg38UCSC Ensembl
chr3:8821591..8860555hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3838965
hg1938965
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425052
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976738
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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