A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718895



Internal ID18670490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14687525..14956129hg38UCSC Ensembl
Innerchr16:14781382..15049986hg19UCSC Ensembl
Innerchr16:14688883..14957487hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38268605
hg19268605
hg18268605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040272
Supporting Variants
Samples
Known GenesABCC6P2, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718895
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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