A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238007



Internal ID20805047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39632380..39632872hg38UCSC Ensembl
chr15:39924581..39925073hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580184
Supporting Variants
Samples
Known GenesFSIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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