A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241013



Internal ID20808053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28600581..28601149hg38UCSC Ensembl
chr17:26927599..26928167hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582795
Supporting Variants
Samples
Known GenesSPAG5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241013
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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