A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358902



Internal ID21016455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21831459..21832917hg38UCSC Ensembl
chr3:21872951..21874409hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381459
hg191459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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