A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6629n223



Internal ID22809597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27711420..27712140hg38UCSC Ensembl
chr7:27751039..27751759hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6575053, nsv6559059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6629n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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