A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046592



Internal ID19135811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54581597hg38UCSC Ensembl
Innerchr11:51537683..51564415hg19UCSC Ensembl
Innerchr11:51394259..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg3826733
hg1926733
hg1826733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1158n100
Supporting Variantsnssv3521027, nssv3508333
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)nsv1046592
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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