A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246752



Internal ID21307265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21580020..21582313hg38UCSC Ensembl
Outerchr16:21580019..21584992hg38UCSC Ensembl
Innerchr16:21591341..21593634hg19UCSC Ensembl
Outerchr16:21591340..21596313hg19UCSC Ensembl
Innerchr16:21498842..21501135hg18UCSC Ensembl
Outerchr16:21498841..21503814hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384974
hg194974
hg184974
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169963
Supporting Variants
SamplesNGO_33
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246752
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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