A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626689



Internal ID15850222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186292301..186294152hg38UCSC Ensembl
Outerchr4:187213455..187215306hg19UCSC Ensembl
Outerchr4:187450449..187452300hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381852
hg191852
hg181852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513190
Supporting Variants
Samples1
Known GenesF11-AS1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626689
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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