A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553064



Internal ID15993787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1943082..2001669hg38UCSC Ensembl
Innerchr11:1964312..2022899hg19UCSC Ensembl
Innerchr11:1920888..1979475hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3858588
hg1958588
hg1858588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174282
Samples1780862275_A
Known GenesH19, MIR675, MRPL23, MRPL23-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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