A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511732



Internal ID22569684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134130828..134145773hg38UCSC Ensembl
chr9:136995950..137010895hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3814946
hg1914946
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855718
Supporting Variants
Samples
Known GenesWDR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511732
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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