A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556102



Internal ID20929173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19256333..19257070hg38UCSC Ensembl
chr9:19256331..19257068hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280302
Samples
Known GenesDENND4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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