A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125769



Internal ID19251289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:9086726..9086805hg38UCSC Ensembl
Outerchr3:9128410..9128489hg19UCSC Ensembl
Cytoband3p25.3
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 Variantsnssv3983973
SamplesKWS2
Known GenesSRGAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125769
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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