A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761305



Internal ID20537165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90702014..90702014hg38UCSC Ensembl
chr5:89997831..89997831hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284963
Samples
Known GenesGPR98
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761305
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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