A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141599



Internal ID19273260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33597202..33600102hg38UCSC Ensembl
Outerchr9:33597200..33600100hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382901
hg192901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993105
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141599
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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