A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233896



Internal ID20800936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15552914..15553982hg38UCSC Ensembl
chr12:15705848..15706916hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381069
hg191069
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577006
Supporting Variants
Samples
Known GenesPTPRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233896
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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