A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587981



Internal ID20961052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21630764..21631141hg38UCSC Ensembl
chr18:19210725..19211102hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587981
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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