A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625120



Internal ID15848656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:14855493..14860952hg38UCSC Ensembl
Outerchr18:14855492..14860951hg19UCSC Ensembl
Outerchr18:14845492..14850951hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg385460
hg195460
hg185460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512518
Supporting Variants
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)nssv625120
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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