A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367453



Internal ID21025006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153341261..153363540hg38UCSC Ensembl
chr3:153059050..153081329hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3822280
hg1922280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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