A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242278



Internal ID20809318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43184373..43185101hg38UCSC Ensembl
chr17:41336390..41337118hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38729
hg19729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588375
Supporting Variants
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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