A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117502



Internal ID19272241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:6258637..6290491hg38UCSC Ensembl
Outerchr9:6258637..6290491hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3831855
hg1931855
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980081
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117502
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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