A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540936



Internal ID20914223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39057680..39058787hg38UCSC Ensembl
chr3:39099171..39100278hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260024
Samples
Known GenesWDR48
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540936
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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