A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6028770



Internal ID21938113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65778453..65788700hg38UCSC Ensembl
chr15:66070791..66081038hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810248
hg1910248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600216
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6028770
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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