A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718969



Internal ID18670564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15281849hg38UCSC Ensembl
Innerchr16:15048756..15375706hg19UCSC Ensembl
Innerchr16:14956257..15283207hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38326951
hg19326951
hg18326951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047178
Supporting Variants
Samples
Known GenesMIR1972-1, MIR1972-2, MIR3180-4, MIR6511B-1, 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)nssv3718969
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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