A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244006



Internal ID21313154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21521901..21582313hg38UCSC Ensembl
Outerchr16:21509217..21584992hg38UCSC Ensembl
Innerchr16:21533222..21593634hg19UCSC Ensembl
Outerchr16:21520538..21596313hg19UCSC Ensembl
Innerchr16:21440723..21501135hg18UCSC Ensembl
Outerchr16:21428039..21503814hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3875776
hg1975776
hg1875776
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169963
Supporting Variants
SamplesSNI_7
Known GenesSLC7A5P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244006
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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