A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006586



Internal ID19095803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91613446hg38UCSC Ensembl
Innerchr2:91618895..91801472hg19UCSC Ensembl
Innerchr2:90982622..91165199hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38186921
hg19182578
hg18182578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579416, nssv3579414, nssv3579415
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)nsv1006586
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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