A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755461



Internal ID20531321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93618730..93618730hg38UCSC Ensembl
chr9:96381012..96381012hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269267
Samples
Known GenesPHF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755461
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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