A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925320



Internal ID22700547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140543674..140543971hg38UCSC Ensembl
chr7:140243474..140243771hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444431
Samples
Known GenesDENND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925320
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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