A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119298



Internal ID19271925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63291128..63373928hg38UCSC Ensembl
Outerchr9:67246100..67328900hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3882801
hg1982801
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959735
SamplesKWS1
Known GenesAQP7P1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119298
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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