A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554002



Internal ID16341411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36003568..36030662hg38UCSC Ensembl
Innerchr11:36025118..36052212hg19UCSC Ensembl
Innerchr11:35981694..36008788hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3827095
hg1927095
hg1827095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771061
Samples
Known GenesLDLRAD3, MIR3973
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554002
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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