A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558539



Internal ID20931610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105688395..105690221hg38UCSC Ensembl
chr7:105328842..105330668hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273558
Samples
Known GenesATXN7L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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