A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2329n223



Internal ID22805297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106219756..106883700hg38UCSC Ensembl
chr14:106676400..107289540hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38663945
hg19613141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6498418, nsv6499078, nsv6502970, nsv6510416
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2329n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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