A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579923



Internal ID20952994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42384133..42385524hg38UCSC Ensembl
chr17:40536151..40537542hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243000
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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