A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv662n223



Internal ID22803630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26579164..26641185hg38UCSC Ensembl
chr10:26868093..26930114hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3862022
hg1962022
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6441192, nsv6437653, nsv6437797
Samples
Known GenesLINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv662n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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