A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219840



Internal ID20786880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71666298..71666962hg38UCSC Ensembl
chr12:72060078..72060742hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592230
Supporting Variants
Samples
Known GenesTHAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00023


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