A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512158



Internal ID15851583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32264334..32267281hg38UCSC Ensembl
Outerchr10:32553262..32556209hg19UCSC Ensembl
Outerchr10:32593268..32596215hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382948
hg192948
hg182948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624721
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)nsv512158
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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