A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110059



Internal ID19273955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:121892144..121892197hg38UCSC Ensembl
Outerchr9:124654423..124654476hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959296
SamplesKWS1
Known GenesTTLL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110059
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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