A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754124



Internal ID20529984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17773688..17856253hg38UCSC Ensembl
chr12:17926622..18009187hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3882566
hg1982566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv22n199
Supporting Variantsnssv16267505
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754124
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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