A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586010



Internal ID20959081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31880895..31881571hg38UCSC Ensembl
chr17:30207914..30208590hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244395
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586010
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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