A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217873



Internal ID20784913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32699713..32700384hg38UCSC Ensembl
chr12:32852647..32853318hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576091
Supporting Variants
Samples
Known GenesDNM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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