A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv39n223



Internal ID22803007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8120801..8132400hg38UCSC Ensembl
chr1:8180861..8192460hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3811600
hg1911600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6335133, nsv6326426, nsv6335102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv39n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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