A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038785



Internal ID18781316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14895994..15014718hg38UCSC Ensembl
Innerchr16:14989851..15108575hg19UCSC Ensembl
Innerchr16:14897352..15016076hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38118725
hg19118725
hg18118725
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2752n100
Supporting Variantsnssv3557635, nssv3557636, nssv3557637
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)nsv1038785
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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