A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv164n223



Internal ID22803132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40108701..40123000hg38UCSC Ensembl
chr1:40574373..40588672hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3814300
hg1914300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6334631, nsv6332791, nsv6331140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv164n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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