A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3556952



Internal ID18508547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1063695..1299208hg38UCSC Ensembl
Innerchr16:1113695..1349209hg19UCSC Ensembl
Innerchr16:1053696..1289210hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38235514
hg19235515
hg18235515
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046885
Supporting Variants
Samples
Known GenesC1QTNF8, CACNA1H, SSTR5, SSTR5-AS1, TPSAB1, TPSB2, TPSD1, TPSG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3556952
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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