A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579798



Internal ID20952869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69513941..69514857hg38UCSC Ensembl
chr17:67510082..67510998hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3238n223
Supporting Variantsnssv18243886
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579798
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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