A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115828



Internal ID19273511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40915718..40991771hg38UCSC Ensembl
Outerchr9:68988900..69065000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3876054
hg1976101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977637
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115828
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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