A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6073n223



Internal ID22809041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17382414..17880550hg38UCSC Ensembl
chr6:17382645..17880781hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38498137
hg19498137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6401059, nsv6415173
Samples
Known GenesCAP2, FAM8A1, KIF13A, NUP153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6073n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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