A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058050



Internal ID19147269
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 StatusM
Merged Variantsdgv2996n100
Supporting Variantsnssv3559442
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)nsv1058050
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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