A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244941



Internal ID20811981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9142789..9143505hg38UCSC Ensembl
chr18:9142787..9143503hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584957
Supporting Variants
Samples
Known GenesANKRD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244941
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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