A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425561



Internal ID22483431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15064523..15064578hg38UCSC Ensembl
chr4:15066147..15066202hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905825
Supporting Variants
Samples
Known GenesCPEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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