A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222448



Internal ID20789488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77381166..77381657hg38UCSC Ensembl
chr12:77774946..77775437hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222448
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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