A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578526



Internal ID20951597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5312857..5314147hg38UCSC Ensembl
chr18:5312856..5314146hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381291
hg191291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3270n223
Supporting Variantsnssv18244659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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