A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559383



Internal ID20932454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36242947..36243647hg38UCSC Ensembl
chr9:36242944..36243644hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7695n223
Supporting Variantsnssv18280617
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559383
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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