A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541643



Internal ID20914925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9921790..9923106hg38UCSC Ensembl
chr3:9963474..9964790hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262771
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541643
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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