A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6631n223



Internal ID22809599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29613971..29615938hg38UCSC Ensembl
chr7:29653587..29655554hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381968
hg191968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6559421, nsv6563231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6631n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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