A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051201



Internal ID18793732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80261889..81448000hg38UCSC Ensembl
Innerchr11:79972933..81159042hg19UCSC Ensembl
Innerchr11:79650581..80836690hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381186112
hg191186110
hg181186110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513652
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)nsv1051201
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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