A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147450



Internal ID19202872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64464681..64467182hg38UCSC Ensembl
Outerchr9:69477099..69479600hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000228
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147450
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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