A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626684



Internal ID15850217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183752943..183756039hg38UCSC Ensembl
Outerchr4:184674096..184677192hg19UCSC Ensembl
Outerchr4:184911090..184914186hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg383097
hg193097
hg183097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513186
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)nssv626684
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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