A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367793



Internal ID21025346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147379721..147382235hg38UCSC Ensembl
chr3:147097508..147100022hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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