A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512602



Internal ID15852027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:4737710..4739974hg38UCSC Ensembl
Outerchr20:4718356..4720620hg19UCSC Ensembl
Outerchr20:4666356..4668620hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382265
hg192265
hg182265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625214
Samples1
Known GenesPRNT
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512602
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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