A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049917



Internal ID19139136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14803932..14993308hg38UCSC Ensembl
Innerchr16:14897789..15087165hg19UCSC Ensembl
Innerchr16:14805290..14994666hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38189377
hg19189377
hg18189377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2744n100
Supporting Variantsnssv3557563, nssv3557562
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)nsv1049917
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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