A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3582208



Internal ID18533803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87110834..87652179hg38UCSC Ensembl
Innerchr2:87337957..87951698hg19UCSC Ensembl
Innerchr2:87191468..87732813hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38541346
hg19613742
hg18541346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009615
Supporting Variants
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3582208
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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