A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557127



Internal ID20930198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179616242..179617455hg38UCSC Ensembl
chr3:179334030..179335243hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261159
Samples
Known GenesNDUFB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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