A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048092



Internal ID19137311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42262915..42305603hg38UCSC Ensembl
Innerchr11:42284465..42327153hg19UCSC Ensembl
Innerchr11:42241041..42283729hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3842689
hg1942689
hg1842689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n100
Supporting Variantsnssv3710116
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)nsv1048092
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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