A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979565



Internal ID22754500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177922860..177929484hg38UCSC Ensembl
chr3:177640648..177647272hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg386625
hg196625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429099
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979565
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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