A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558145



Internal ID20931216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13674955..13675994hg38UCSC Ensembl
chr9:13674954..13675993hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg381040
hg191040
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7622n223
Supporting Variantsnssv18280161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558145
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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