A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054731



Internal ID18797262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14877546..15414043hg38UCSC Ensembl
Innerchr16:14971403..15507900hg19UCSC Ensembl
Innerchr16:14878904..15415401hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38536498
hg19536498
hg18536498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2755n100
Supporting Variantsnssv3557595
Samples
Known GenesLOC100288162, MIR1972-1, MIR1972-2, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR6511A-2, MIR6511B-1, MIR6770-2, MPV17L, NOMO1, NPIPA1, NPIPA5, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054731
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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