A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6662n223



Internal ID22809630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:48861390..48910690hg38UCSC Ensembl
chr7:48900986..48950286hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3849301
hg1949301
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6561905, nsv6568928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6662n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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