A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557797



Internal ID18509392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15322641hg38UCSC Ensembl
Innerchr16:15048756..15416498hg19UCSC Ensembl
Innerchr16:14956257..15323999hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38367743
hg19367743
hg18367743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036878
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)nssv3557797
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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