A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6906n223



Internal ID22809874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72499748..72864951hg38UCSC Ensembl
chr7:71964733..72335515hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38365204
hg19370783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6610049, nsv6607159
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, SPDYE7P, TYW1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6906n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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