A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999595



Internal ID18846396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:14326781..14327087hg38UCSC Ensembl
Outerchr11:14348327..14348633hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146392
Supporting Variants
SamplesKWB1
Known GenesRRAS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999595
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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