A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718906



Internal ID19017187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..14983611hg38UCSC Ensembl
Innerchr16:14888583..15077468hg19UCSC Ensembl
Innerchr16:14796084..14984969hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38188886
hg19188886
hg18188886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052916
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718906
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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