A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559534



Internal ID332566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123466378..123467527hg38UCSC Ensembl
chr9:126228657..126229806hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381150
hg191150
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027175
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559534
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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