A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591846



Internal ID20964917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11534018..11535140hg38UCSC Ensembl
chr17:11437335..11438457hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240984
Samples
Known GenesSHISA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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