A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049292



Internal ID19138511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:135022781..135074876hg38UCSC Ensembl
Innerchr11:134892675..134944770hg19UCSC Ensembl
Innerchr11:134397885..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3852096
hg1952096
hg1852098
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1321n100
Supporting Variantsnssv3710801, nssv3502811, nssv3710800, nssv3518074
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)nsv1049292
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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