A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375234



Internal ID21032787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18597418..18624279hg38UCSC Ensembl
chr3:18638910..18665771hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3826862
hg1926862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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