A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046238



Internal ID18788769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16764451..17658452hg38UCSC Ensembl
Innerchr16:16858308..17752309hg19UCSC Ensembl
Innerchr16:16765809..17659810hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38894002
hg19894002
hg18894002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3558095
Samples
Known GenesXYLT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046238
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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