A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559777



Internal ID18858058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79557382..79580271hg38UCSC Ensembl
Innerchr16:79591279..79614168hg19UCSC Ensembl
Innerchr16:78148780..78171669hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3822890
hg1922890
hg1822890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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