A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758504



Internal ID20534364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101509160..101509160hg38UCSC Ensembl
chr8:102521388..102521388hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267886
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758504
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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