A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561140



Internal ID20934211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153017977..153018770hg38UCSC Ensembl
chr3:152735766..152736559hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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