A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718923



Internal ID18670518
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055110
Supporting Variants
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)nssv3718923
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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