A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217549



Internal ID20784589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48669596..48669995hg38UCSC Ensembl
chr12:49063379..49063778hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575935
Supporting Variants
Samples
Known GenesKANSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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