A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989743



Internal ID18888456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:90075532..90090132hg38UCSC Ensembl
Outerchr11:89808700..89823300hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3814601
hg1914601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136138
Supporting Variants
SamplesKWS2
Known GenesUBTFL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989743
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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