A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574218



Internal ID20947289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16561648..16561798hg38UCSC Ensembl
chr6:16561879..16562029hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269939
Samples
Known GenesATXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574218
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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