A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553984



Internal ID15994707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31433428..31632859hg38UCSC Ensembl
Innerchr11:31454975..31654406hg19UCSC Ensembl
Innerchr11:31411551..31610982hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38199432
hg19199432
hg18199432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1740n54
Supporting Variantsnssv771042
Samples
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553984
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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