A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624615



Internal ID15848151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:117861441..117863685hg38UCSC Ensembl
Outerchr8:118873680..118875924hg19UCSC Ensembl
Outerchr8:118942861..118945105hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg382245
hg192245
hg182245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512062
Supporting Variants
Samples1
Known GenesEXT1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624615
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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