A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756603



Internal ID20532463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66691507..66691507hg38UCSC Ensembl
chr8:67603742..67603742hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286776
Samples
Known GenesC8orf44-SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756603
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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