A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3005n223



Internal ID22805973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15145301..15157000hg38UCSC Ensembl
chr17:15048618..15060317hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6496281, nsv6502853, nsv6495606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3005n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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