A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045013



Internal ID18787544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16149597..16170241hg38UCSC Ensembl
Innerchr16:16243454..16264098hg19UCSC Ensembl
Innerchr16:16150955..16171599hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3820645
hg1920645
hg1820645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718986
Samples
Known GenesABCC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045013
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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