A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1609n54



Internal ID22769504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5738876..5740096hg38UCSC Ensembl
chr11:5760106..5761326hg19UCSC Ensembl
chr11:5716682..5717902hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381221
hg191221
hg181221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553289, nsv553280, nsv553281
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1609n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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