A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063303



Internal ID19152522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35224654..35521183hg38UCSC Ensembl
Innerchr16:34459025..34755554hg19UCSC Ensembl
Innerchr16:34316526..34613055hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38296530
hg19296530
hg18296530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3556043, nssv3556048, nssv3556042, nssv3556047, nssv3556046, nssv3556050, nssv3722224, nssv3722225, nssv3556049, nssv3556045, nssv3556044, nssv3556041
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063303
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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