A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625046



Internal ID15501896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87999010..88001262hg38UCSC Ensembl
Outerchr16:88032616..88034868hg19UCSC Ensembl
Outerchr16:86590117..86592369hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382253
hg192253
hg182253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512450
Supporting Variants
Samples1
Known GenesBANP
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625046
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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