A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758132



Internal ID20533992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:63287356..63287356hg38UCSC Ensembl
chr15:63579555..63579555hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269099
Samples
Known GenesAPH1B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758132
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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