A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243699



Internal ID20810740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58972659..58973355hg38UCSC Ensembl
chr17:57050020..57050716hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582820
Supporting Variants
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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