A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040161



Internal ID19129380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39343935..39386915hg38UCSC Ensembl
Innerchr11:39365485..39408465hg19UCSC Ensembl
Innerchr11:39322061..39365041hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3842981
hg1942981
hg1842981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1104n100
Supporting Variantsnssv3710114
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)nsv1040161
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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