A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565203



Internal ID20938274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19244320..19244473hg38UCSC Ensembl
chr9:19244318..19244471hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280301
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565203
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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