A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv513n223



Internal ID22803481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206005101..206026700hg38UCSC Ensembl
chr1:206314668..206332221hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3821600
hg1917554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6321688, nsv6321102
Samples
Known GenesCTSE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv513n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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