A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556951



Internal ID18508546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1002943..1394728hg38UCSC Ensembl
Innerchr16:1052943..1444729hg19UCSC Ensembl
Innerchr16:992944..1384730hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38391786
hg19391787
hg18391787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039643
Supporting Variants
Samples
Known GenesBAIAP3, C1QTNF8, CACNA1H, GNPTG, SSTR5, SSTR5-AS1, TPSAB1, TPSB2, TPSD1, TPSG1, TSR3, UBE2I, UNKL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556951
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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