A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4785n223



Internal ID22807753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7798105..7950063hg38UCSC Ensembl
chr3:7839792..7991750hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38151959
hg19151959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6373888, nsv6372079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4785n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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