A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431704



Internal ID21393706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16267190..16268493hg38UCSC Ensembl
chr12:16420124..16421427hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv161n172
Supporting Variantsnssv15745891
SamplesMDQ025
Known GenesSLC15A5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431704
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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