A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558666



Internal ID20931737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107220949..107221765hg38UCSC Ensembl
chr7:106861394..106862210hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273584
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558666
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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