A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036277



Internal ID18778808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7133989..7163616hg38UCSC Ensembl
Innerchr16:7183990..7213617hg19UCSC Ensembl
Innerchr16:7123991..7153618hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3829628
hg1929628
hg1829628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557077
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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