A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219003



Internal ID20786043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9857689..9858810hg38UCSC Ensembl
chr12:10010288..10011409hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578311
Supporting Variants
Samples
Known GenesCLEC2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219003
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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