A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566258



Internal ID20939329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158454609..158455447hg38UCSC Ensembl
chr6:158875641..158876479hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38839
hg19839
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270467
Samples
Known GenesTULP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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