A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995668



Internal ID21905011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15470667..15470723hg38UCSC Ensembl
chr4:15472291..15472347hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547629
Samples
Known GenesCC2D2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995668
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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