A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242095



Internal ID20809135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18029599..18030321hg38UCSC Ensembl
chr17:17932913..17933635hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591667
Supporting Variants
Samples
Known GenesATPAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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