A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6637n223



Internal ID22809605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32725501..32774500hg38UCSC Ensembl
chr7:32765113..32814112hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3849000
hg1949000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6615478, nsv6608555
Samples
Known GenesLINC00997, MIR550A2, MIR550B2, ZNRF2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6637n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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