A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236719



Internal ID20803759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104040494..104041132hg38UCSC Ensembl
chr12:104434272..104434910hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594468
Supporting Variants
Samples
Known GenesGLT8D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236719
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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