A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6900n223



Internal ID22809868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71537196..72263841hg38UCSC Ensembl
chr7:71002181..71728826hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38726646
hg19726646
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6602108, nsv6613749
Samples
Known GenesCALN1, WBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6900n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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