A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626641



Internal ID15850174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87999354..88000601hg38UCSC Ensembl
Outerchr4:88920506..88921753hg19UCSC Ensembl
Outerchr4:89139530..89140777hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg381248
hg191248
hg181248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513147
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)nssv626641
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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