A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549410



Internal ID20922572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25644476..25644858hg38UCSC Ensembl
chr3:25685967..25686349hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262611
Samples
Known GenesTOP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549410
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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