A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1864n223



Internal ID22804832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61032991..61065153hg38UCSC Ensembl
chr13:61607125..61639287hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3832163
hg1932163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6493523, nsv6483965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1864n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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