A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957172



Internal ID17306045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9302132..9303183hg38UCSC Ensembl
Outerchr11:9323679..9324730hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004990
SamplesBILGI_BIOE
Known GenesTMEM41B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957172
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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