A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755685



Internal ID20531545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80974185..80974185hg38UCSC Ensembl
chr15:81266526..81266526hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755685
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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