A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951072



Internal ID16953259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:113689879..113690778hg38UCSC Ensembl
Outerchr11:113560601..113561500hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999619
SamplesBILGI_BIOE
Known GenesTMPRSS5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951072
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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