A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560281



Internal ID20933352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123588581..123589068hg38UCSC Ensembl
chr9:126350860..126351347hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279805
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560281
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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