A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855718



Internal ID22630653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134130828..134145773hg38UCSC Ensembl
chr9:136995950..137010895hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3814946
hg1914946
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511732
Samples
Known GenesWDR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855718
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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