A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240969



Internal ID20808009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10727922..10728315hg38UCSC Ensembl
chr17:10631239..10631632hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592671
Supporting Variants
Samples
Known GenesTMEM220
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240969
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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