A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6600n223



Internal ID22809568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15667015..15668495hg38UCSC Ensembl
chr7:15706640..15708120hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6558035, nsv6562711
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6600n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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