A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999581



Internal ID17292533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:69808933..69820332hg38UCSC Ensembl
Outerchr11:69623701..69635100hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951034
Supporting Variants
SamplesBILGI_BIOE
Known GenesFGF3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999581
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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