A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757526



Internal ID20533386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101009900..101009900hg38UCSC Ensembl
chr14:101476237..101476237hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757526
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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