A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576008



Internal ID20949079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31698899..31699514hg38UCSC Ensembl
chr18:29278862..29279477hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3339n223
Supporting Variantsnssv18244033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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