A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745891



Internal ID21386613
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 StatusS
Merged Variantsnsv4431704
Supporting Variants
SamplesMDQ025
Known GenesSLC15A5
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745891
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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