A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011451



Internal ID19100668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91681308hg38UCSC Ensembl
Innerchr2:91618895..91869334hg19UCSC Ensembl
Innerchr2:90982622..91233061hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38254783
hg19250440
hg18250440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3991n100
Supporting Variantsnssv3579438
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011451
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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