A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7334n223



Internal ID22810302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50227801..50229700hg38UCSC Ensembl
chr8:51140361..51142260hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6417170, nsv6420592
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7334n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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