A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585865



Internal ID20958936
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 StatusM
Merged Variants
Supporting Variantsnssv18243883
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585865
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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