A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626509



Internal ID15503356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:133546..136894hg38UCSC Ensembl
Outerchr3:175229..178577hg19UCSC Ensembl
Outerchr3:150229..153577hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383349
hg193349
hg183349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513028
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)nssv626509
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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