A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553987



Internal ID15994710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31467343..31674788hg38UCSC Ensembl
Innerchr11:31488890..31696336hg19UCSC Ensembl
Innerchr11:31445466..31652912hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38207446
hg19207447
hg18207447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1740n54
Supporting Variantsnssv1174615
SamplesHGDP00106
Known GenesELP4, IMMP1L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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