A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv565n223



Internal ID22803533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238319701..238323327hg38UCSC Ensembl
chr1:238483001..238486627hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg383627
hg193627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6319370, nsv6327986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv565n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer