A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755280



Internal ID20531140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93150252..93150252hg38UCSC Ensembl
chr8:94162481..94162481hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293955
Samples
Known GenesC8orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755280
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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