A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595278



Internal ID20968349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2668507..2669330hg38UCSC Ensembl
chr17:2571801..2572624hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241600
Samples
Known GenesPAFAH1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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