A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626799



Internal ID15503646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:601158..602999hg38UCSC Ensembl
Outerchr6:601158..602999hg19UCSC Ensembl
Outerchr6:546158..547999hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381842
hg191842
hg181842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513289
Supporting Variants
Samples1
Known GenesEXOC2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626799
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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