A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575913



Internal ID20948984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:48806125..48807882hg38UCSC Ensembl
chr17:46883487..46885244hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244477
Samples
Known GenesTTLL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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