A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219506



Internal ID20786546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95305602..95306841hg38UCSC Ensembl
chr12:95699378..95700617hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219506
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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