A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512601



Internal ID15852026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:1579329..1615431hg38UCSC Ensembl
Outerchr20:1559975..1596077hg19UCSC Ensembl
Outerchr20:1507975..1544077hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836103
hg1936103
hg1836103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625213
Samples1
Known GenesSIRPB1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512601
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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