A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040869



Internal ID19130088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81274905..81307644hg38UCSC Ensembl
Innerchr11:80985948..81018687hg19UCSC Ensembl
Innerchr11:80663596..80696335hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3832740
hg1932740
hg1832740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3506259
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)nsv1040869
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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