A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866056



Internal ID22640991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134156411..134161060hg38UCSC Ensembl
chr9:137021533..137026182hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg384650
hg194650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511738
Samples
Known GenesWDR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866056
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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