A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559968



Internal ID20933039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10936885..10937302hg38UCSC Ensembl
chr7:10976512..10976929hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273630
Samples
Known GenesNDUFA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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