A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014180



Internal ID19103400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:146106824..146143926hg38UCSC Ensembl
Innerchr2:146864392..146901494hg19UCSC Ensembl
Innerchr2:146580862..146617964hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3837103
hg1937103
hg1837103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582938
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014180
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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