A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577987



Internal ID20951058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26055021..26055333hg38UCSC Ensembl
chr18:23634985..23635297hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246847
Samples
Known GenesSS18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577987
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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