A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029444



Internal ID21938787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87083340..87083401hg38UCSC Ensembl
chr14:87549684..87549745hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029444
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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