A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369092



Internal ID21026645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:29968001..29978600hg38UCSC Ensembl
chr3:30009492..30020091hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3810600
hg1910600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102111
Samples
Known GenesRBMS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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