A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051107



Internal ID19140326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37746263..37821374hg38UCSC Ensembl
Innerchr11:37767813..37842924hg19UCSC Ensembl
Innerchr11:37724389..37799500hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3875112
hg1975112
hg1875112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1101n100
Supporting Variantsnssv3515038, nssv3509402
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)nsv1051107
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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