A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626577



Internal ID15850110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:154930105..154932776hg38UCSC Ensembl
Outerchr3:154647894..154650565hg19UCSC Ensembl
Outerchr3:156130588..156133259hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg382672
hg192672
hg182672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513089
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626577
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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