A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050475



Internal ID18793006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15562515..15599056hg38UCSC Ensembl
Innerchr11:15584061..15620602hg19UCSC Ensembl
Innerchr11:15540637..15577178hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3836542
hg1936542
hg1836542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520932
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)nsv1050475
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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