A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559956



Internal ID20933027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36243066..36244946hg38UCSC Ensembl
chr9:36243063..36244943hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280619
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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