A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559442



Internal ID18857723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68144536..68207851hg38UCSC Ensembl
Innerchr16:68178439..68241754hg19UCSC Ensembl
Innerchr16:66735940..66799255hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3863316
hg1963316
hg1863316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058050
Supporting Variants
Samples
Known GenesNFATC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559442
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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