A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036772



Internal ID18779303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14869830..15000839hg38UCSC Ensembl
Innerchr16:14963687..15094696hg19UCSC Ensembl
Innerchr16:14871188..15002197hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38131010
hg19131010
hg18131010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2753n100
Supporting Variantsnssv3718918
Samples
Known GenesLOC100288162, 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)nsv1036772
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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