A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557098



Internal ID18855379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8081251..8127624hg38UCSC Ensembl
Innerchr16:8131253..8177626hg19UCSC Ensembl
Innerchr16:8071254..8117627hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3846374
hg1946374
hg1846374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043406
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)nssv3557098
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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