A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755255



Internal ID20531115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6762001..6762001hg38UCSC Ensembl
chr4:6763728..6763728hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755255
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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