A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118209



Internal ID18908716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:35618152..35619052hg38UCSC Ensembl
Outerchr11:35639700..35640600hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980878
SamplesKWS1
Known GenesFJX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118209
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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