A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239157



Internal ID20806197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99215031..99215464hg38UCSC Ensembl
chr15:99755236..99755669hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593185
Supporting Variants
Samples
Known GenesTTC23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239157
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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