A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066465



Internal ID19155684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35517881hg38UCSC Ensembl
Innerchr16:34470704..34752252hg19UCSC Ensembl
Innerchr16:34328205..34609753hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38281549
hg19281549
hg18281549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558452, nssv3558453, nssv3558450, nssv3558454, nssv3558451, nssv3722503, nssv3558446, nssv3722501, nssv3722502, nssv3558449, nssv3558447, nssv3558448, nssv3722500, nssv3722499
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)nsv1066465
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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