A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559295



Internal ID20932366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63351486..63352647hg38UCSC Ensembl
chr6:64061391..64062552hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271637
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559295
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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