A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583954



Internal ID20957025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56839964..56840439hg38UCSC Ensembl
chr17:54917325..54917800hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245949
Samples
Known GenesDGKE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583954
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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