A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243883



Internal ID20810923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69435307..69435859hg38UCSC Ensembl
chr17:67431448..67432000hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585865
Supporting Variants
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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