A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129053



Internal ID19281714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:85071385..85077385hg38UCSC Ensembl
Outerchr9:87686300..87692300hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961726
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129053
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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