A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369309



Internal ID21026862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148103486..148105361hg38UCSC Ensembl
chr3:147821273..147823148hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381876
hg191876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369309
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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