A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293955



Internal ID20503173
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 StatusS
Merged Variantsnsv4755280
Supporting Variants
Samples
Known GenesC8orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293955
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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