A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560227



Internal ID20933298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7346927..7356869hg38UCSC Ensembl
chr6:7347160..7357102hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg389943
hg199943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274091
Samples
Known GenesCAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560227
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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