A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129026



Internal ID18911654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39107617..39109727hg38UCSC Ensembl
Outerchr9:65626100..65628200hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382111
hg192101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961698
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129026
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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