A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600216



Internal ID21792263
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 StatusS
Merged Variantsnsv6028770
Supporting Variants
Samples
Known GenesDENND4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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