A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014226



Internal ID18756760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:232362777..232378950hg38UCSC Ensembl
Innerchr2:233227487..233243660hg19UCSC Ensembl
Innerchr2:232935731..232951904hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3816174
hg1916174
hg1816174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586889
Samples
Known GenesALPP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014226
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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