A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152680



Internal ID19202358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:115095589..115095648hg38UCSC Ensembl
Outerchr9:117857868..117857927hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999860
SamplesKWB1
Known GenesTNC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152680
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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