A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010669



Internal ID18753201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127091284..127274970hg38UCSC Ensembl
Innerchr2:127848860..128032546hg19UCSC Ensembl
Innerchr2:127565330..127749016hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38183687
hg19183687
hg18183687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4066n100
Supporting Variantsnssv3580749
Samples
Known GenesBIN1, CYP27C1, ERCC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010669
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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