A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952454



Internal ID16954641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57754529..57755028hg38UCSC Ensembl
Outerchr11:57522001..57522500hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999549
SamplesBILGI_BIOE
Known GenesTMX2-CTNND1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952454
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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