A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266693



Internal ID20833733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1338185..1502373hg38UCSC Ensembl
chr5:1338300..1502488hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38164189
hg19164189
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562912
Supporting Variants
Samples
Known GenesCLPTM1L, LPCAT1, SLC6A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266693
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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