A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567717



Internal ID20940788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136704557..136706268hg38UCSC Ensembl
chr6:137025695..137027406hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272399
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567717
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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