A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110415



Internal ID19265694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81013949..81015549hg38UCSC Ensembl
Outerchr3:81063100..81064700hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960066
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110415
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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