A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423982



Internal ID22481852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180679428..180679483hg38UCSC Ensembl
chr3:180397216..180397271hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905324
Supporting Variants
Samples
Known GenesCCDC39
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423982
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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