A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241747



Internal ID20808787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30125190..30125571hg38UCSC Ensembl
chr17:28452208..28452589hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578793
Supporting Variants
Samples
Known GenesNSRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00027


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