A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563401



Internal ID20936472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153435539..153436756hg38UCSC Ensembl
chr3:153153328..153154545hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381218
hg191218
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563401
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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