A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757159



Internal ID20533019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73820476..73820476hg38UCSC Ensembl
chr10:75580234..75580234hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272208
Samples
Known GenesCAMK2G
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757159
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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