A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718912



Internal ID18670507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14794726..15031584hg38UCSC Ensembl
Innerchr16:14888583..15125441hg19UCSC Ensembl
Innerchr16:14796084..15032942hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38236859
hg19236859
hg18236859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051136
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR1972-1, MIR1972-2, 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)nssv3718912
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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