A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1740n54



Internal ID20135164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31433428..31674788hg38UCSC Ensembl
chr11:31454975..31696336hg19UCSC Ensembl
chr11:31411551..31652912hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38241361
hg19241362
hg18241362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553985, nsv553986, nsv553987, nsv553984
SamplesHGDP00106
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1740n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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