A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567463



Internal ID20940534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136603201..136604110hg38UCSC Ensembl
chr6:136924339..136925248hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38910
hg19910
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272394
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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