A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136036



Internal ID19259946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57807220..57809220hg38UCSC Ensembl
Outerchr11:57574692..57576692hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994214, nssv3968363
SamplesKWS2, KWS1
Known GenesCTNND1, TMX2-CTNND1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136036
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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