A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7132n223



Internal ID22810100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139134408..139135104hg38UCSC Ensembl
chr7:138819154..138819850hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6565501, nsv6566067
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7132n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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