A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055110



Internal ID18797641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14887108..15022388hg38UCSC Ensembl
Innerchr16:14980965..15116245hg19UCSC Ensembl
Innerchr16:14888466..15023746hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38135281
hg19135281
hg18135281
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2752n100
Supporting Variantsnssv3557605, nssv3718922, nssv3557607, nssv3557606, nssv3718923
Samples
Known GenesLOC100288162, 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)nsv1055110
Frequency
Sample Size29084
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer