A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565082



Internal ID20938153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148985738..148987103hg38UCSC Ensembl
chr3:148703525..148704890hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262574
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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