A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6602n223



Internal ID22809570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16875809..17377200hg38UCSC Ensembl
chr7:16915433..17416824hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38501392
hg19501392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6616677, nsv6610318
Samples
Known GenesAGR3, AHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6602n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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