A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512179



Internal ID15504918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97275017..97277637hg38UCSC Ensembl
Outerchr10:99034774..99037394hg19UCSC Ensembl
Outerchr10:99024764..99027384hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382621
hg192621
hg182621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624745
Samples1
Known GenesARHGAP19, ARHGAP19-SLIT1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512179
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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