A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045568



Internal ID19134787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21979340..22003931hg38UCSC Ensembl
Innerchr11:22000886..22025477hg19UCSC Ensembl
Innerchr11:21957462..21982053hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3824592
hg1924592
hg1824592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515347
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)nsv1045568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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