A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052916



Internal ID19142135
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 StatusM
Merged Variantsdgv2744n100
Supporting Variantsnssv3718906
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)nsv1052916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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