A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999594



Internal ID17292546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:79190456..79191955hg38UCSC Ensembl
Outerchr11:78901501..78903000hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951047
Supporting Variants
SamplesBILGI_BIOE
Known GenesTENM4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999594
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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