A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569114



Internal ID20942185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136699821..136702707hg38UCSC Ensembl
chr6:137020959..137023845hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382887
hg192887
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272398
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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