A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238898



Internal ID20805938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65531561..65532355hg38UCSC Ensembl
chr15:65823899..65824693hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587616
Supporting Variants
Samples
Known GenesPTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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