A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048367



Internal ID19137586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134753995..134904951hg38UCSC Ensembl
Innerchr11:134623889..134774845hg19UCSC Ensembl
Innerchr11:134129099..134280055hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38150957
hg19150957
hg18150957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3510832
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)nsv1048367
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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