A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624752



Internal ID15501602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112395286..112398854hg38UCSC Ensembl
Outerchr10:114155044..114158612hg19UCSC Ensembl
Outerchr10:114145034..114148602hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg383569
hg193569
hg183569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512186
Supporting Variants
Samples1
Known GenesACSL5
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624752
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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