A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244214



Internal ID20811254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36165942..36166594hg38UCSC Ensembl
chr18:33745905..33746557hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583998
Supporting Variants
Samples
Known GenesELP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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