A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129826



Internal ID19278779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97742102..97742198hg38UCSC Ensembl
Outerchr9:100504384..100504480hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3964933
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129826
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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