A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512168



Internal ID15851593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:62946462..62948707hg38UCSC Ensembl
Outerchr10:64706222..64708467hg19UCSC Ensembl
Outerchr10:64376228..64378473hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg382246
hg192246
hg182246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624732
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512168
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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