A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580281



Internal ID18878562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117017795..117176362hg38UCSC Ensembl
Innerchr2:117775371..117933938hg19UCSC Ensembl
Innerchr2:117491841..117650408hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38158568
hg19158568
hg18158568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001398
Supporting Variants
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)nssv3580281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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