A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762689



Internal ID20538549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101226877..101226877hg38UCSC Ensembl
chr14:101693214..101693214hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762689
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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