A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592797



Internal ID20965868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10650174..10650908hg38UCSC Ensembl
chr17:10553491..10554225hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240965
Samples
Known GenesMYH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592797
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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