A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1855n223



Internal ID22804823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:57635201..57676700hg38UCSC Ensembl
chr13:58209335..58250834hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3841500
hg1941500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6485981, nsv6475969
Samples
Known GenesPCDH17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1855n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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