A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6967n223



Internal ID22809935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77251040..77251881hg38UCSC Ensembl
chr7:76880357..76881198hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560953, nsv6563012
Samples
Known GenesCCDC146
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6967n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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