A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559257



Internal ID20932328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107215454..107215776hg38UCSC Ensembl
chr7:106855899..106856221hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273583
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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