A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060105



Internal ID18802636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28112249..28254967hg38UCSC Ensembl
Innerchr16:28123570..28266288hg19UCSC Ensembl
Innerchr16:28031071..28173789hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38142719
hg19142719
hg18142719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549142
Samples
Known GenesXPO6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060105
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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