A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040291



Internal ID19129510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88005993..88065472hg38UCSC Ensembl
Innerchr11:87739161..87798640hg19UCSC Ensembl
Innerchr11:87378809..87438288hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3859480
hg1959480
hg1859480
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3511910
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)nsv1040291
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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