A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242919



Internal ID20809959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39414078..39414626hg38UCSC Ensembl
chr17:37570331..37570879hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581780
Supporting Variants
Samples
Known GenesMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242919
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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