A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886220



Internal ID22661206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42737360..42739146hg38UCSC Ensembl
chr17:40889378..40891164hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381787
hg191787
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473807
Samples
Known GenesEZH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886220
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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