A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128875



Internal ID19285761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:144504958..144506558hg38UCSC Ensembl
Outerchr3:144223800..144225400hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961544
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128875
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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