A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252192



Internal ID21303551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21521901..21580019hg38UCSC Ensembl
Outerchr16:21509217..21582134hg38UCSC Ensembl
Innerchr16:21533222..21591340hg19UCSC Ensembl
Outerchr16:21520538..21593455hg19UCSC Ensembl
Innerchr16:21440723..21498841hg18UCSC Ensembl
Outerchr16:21428039..21500956hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3872918
hg1972918
hg1872918
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169963
Supporting Variants
SamplesMLY_7
Known GenesSLC7A5P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252192
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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