A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359141



Internal ID21016694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153177497..153179513hg38UCSC Ensembl
chr3:152895286..152897302hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096044
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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