A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249630



Internal ID21310123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21580020..21591309hg38UCSC Ensembl
Outerchr16:21580019..21594646hg38UCSC Ensembl
Innerchr16:21591341..21602630hg19UCSC Ensembl
Outerchr16:21591340..21605967hg19UCSC Ensembl
Innerchr16:21498842..21510131hg18UCSC Ensembl
Outerchr16:21498841..21513468hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg3814628
hg1914628
hg1814628
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169963
Supporting Variants
SamplesNGO_55
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249630
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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