A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225610



Internal ID20792650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112486003..112487318hg38UCSC Ensembl
chr12:112923807..112925122hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592481
Supporting Variants
Samples
Known GenesPTPN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225610
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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