A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581664



Internal ID20954735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26410172..26410614hg38UCSC Ensembl
chr18:23990136..23990578hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581664
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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