A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125969



Internal ID19284248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87033895..87033974hg38UCSC Ensembl
Outerchr9:89648810..89648889hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984178
SamplesKWS2
Known GenesLOC440173
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125969
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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