A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548669



Internal ID20921853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39495705..39496971hg38UCSC Ensembl
chr3:39537196..39538462hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260614
Samples
Known GenesMOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548669
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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