A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582731



Internal ID20955802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42332072..42332460hg38UCSC Ensembl
chr17:40484090..40484478hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18242999
Samples
Known GenesSTAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582731
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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