A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239141



Internal ID20806181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98107569..99002946hg38UCSC Ensembl
chr15:98650798..99546175hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38895378
hg19895378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580865
Supporting Variants
Samples
Known GenesFAM169B, IGF1R, MIR4714, PGPEP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239141
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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