A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139949



Internal ID18914038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33385202..33398602hg38UCSC Ensembl
Outerchr9:33385200..33398600hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813401
hg1913401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978285
SamplesKWS2
Known GenesAQP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139949
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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